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- Medical Device Recalls and Early Alerts | FDA
The FDA posts information about certain medical device recalls and early alerts to help increase awareness of these issues
- Medline | Recalls
log in to Medline com to view all Recalls Cookie Preferences Consumer Rights Do Not Sell Or Share My Personal Information Privacy
- MEDLINE NEURO SPONGE - BEUDAMED
FDA 510 (k) clearance for medical device MEDLINE NEURO SPONGE, FDA class 2, K number K140369 Decision: Substantially Equivalent
- Recalls. gov
Follow the tabs above to obtain the latest recall information, to report a dangerous product, or to learn important safety tips
- Recalls, Market Withdrawals, Safety Alerts | FDA
Recalls, Market Withdrawals, Safety Alerts The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products
- Medline Neuro Sponge 510 (k) FDA Premarket Notification K140369 MEDLINE . . .
The following data is part of a premarket notification filed by Medline Industries, Inc with the FDA for Medline Neuro Sponge
- AccessGUDID - DEVICE: MEDLINE (10197344111572)
Brand Name: MEDLINE Version or Model: NEUROSPNG02 Commercial Distribution Status: In Commercial Distribution Catalog Number: NEUROSPNG02 Company Name: MEDLINE INDUSTRIES, INC Primary DI Number: 10197344111572 Issuing Agency: GS1 Commercial Distribution End Date: Device Count: 10 Labeler D-U-N-S® Number*: 025460908 * Terms of Use
- Device Recalls - California Department of Public Health
Information regarding device recalls and links to other device recall information may be found below For any questions, please contact us using the information on the left or email us as the following address: FDBMedDevice@cdph ca gov
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