510(k) K863932
K863932 is an FDA 510(k) premarket notification submitted by Fraass Survival Systems, Inc. for the device "GAUZE, ABSORBENT, STERILE, COMPRESSED". The FDA issued a decision of Substantially Equivalent on October 24, 1986. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Fraass Survival Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 24, 1986
- Date Received
- October 8, 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