510(k) K922735
K922735 is an FDA 510(k) premarket notification submitted by Carl Zeiss, Inc. for the device "ZIESS ENDOPROBE". The FDA issued a decision of Substantially Equivalent on July 9, 1992. The device falls under product code HQB (Photocoagulator And Accessories), a Class II device regulated under 21 CFR 886.4690. Carl Zeiss, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 9, 1992
- Date Received
- June 8, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Photocoagulator And Accessories
- Device Class
- Class II
- Regulation Number
- 886.4690
- Review Panel
- OP
- Submission Type