510(k) K935881
K935881 is an FDA 510(k) premarket notification submitted by Mcneil Healthcare, Inc. for the device "SPECIALTY SPONGES". The FDA issued a decision of Substantially Equivalent on Jan 31, 1994. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. Mcneil Healthcare, Inc. has 18 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 31, 1994
- Date Received
- Dec 9, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Gauze/Sponge, Internal, X-Ray Detectable
- Device Class
- Class I
- Regulation Number
- 878.4450
- Review Panel
- SU
- Submission Type
- 510(k) Exempt