510(k) K852412
K852412 is an FDA 510(k) premarket notification submitted by American White Cross, Inc. for the device "NON-ADHERENT PAD". The FDA issued a decision of Substantially Equivalent on July 29, 1985. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. American White Cross, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 29, 1985
- Date Received
- June 6, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Gauze/Sponge, Internal
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type