510(k) K930496
K930496 is an FDA 510(k) premarket notification submitted by Birtcher Medical Systems, Inc. for the device "GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS". The FDA issued a decision of Substantially Equivalent on April 20, 1993. The device falls under product code GCI (Laryngoscope, Endoscope), a Class II device regulated under 21 CFR 876.1500. Birtcher Medical Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 20, 1993
- Date Received
- February 1, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Laryngoscope, Endoscope
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- SU
- Submission Type