510(k) K934971
K934971 is an FDA 510(k) premarket notification submitted by Medsurg Industries, Inc. for the device "STERILE LAPAROTOMY SPONGES". The FDA issued a decision of Substantially Equivalent on February 7, 1994. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. Medsurg Industries, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 7, 1994
- Date Received
- October 18, 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