510(k) K862126
K862126 is an FDA 510(k) premarket notification submitted by Anago, Inc. for the device "STERILE LAPAROTOMY GAUZE SPONGE". The FDA issued a decision of Substantially Equivalent on June 19, 1986. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Anago, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 19, 1986
- Date Received
- June 4, 1986
- 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