510(k) K874241
K874241 is an FDA 510(k) premarket notification submitted by Carl Zeiss, Inc. for the device "OPMI MD SURGICAL MICROSCOPE". The FDA issued a decision of Substantially Equivalent on December 23, 1987. The device falls under product code FSO (Microscope, Surgical, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4700. Carl Zeiss, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 23, 1987
- Date Received
- October 15, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Microscope, Surgical, General & Plastic Surgery
- Device Class
- Class I
- Regulation Number
- 878.4700
- Review Panel
- SU
- Submission Type