510(k) K882269
K882269 is an FDA 510(k) premarket notification submitted by Storz Instrument Co. for the device "STORZ DIAGNOSTIC MICROSCOPE SYSTEM". The FDA issued a decision of Substantially Equivalent on June 23, 1988. The device falls under product code EPT (Microscope, Surgical), a Class I device regulated under 21 CFR 878.4700. Storz Instrument Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 23, 1988
- Date Received
- May 31, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Microscope, Surgical
- Device Class
- Class I
- Regulation Number
- 878.4700
- Review Panel
- SU
- Submission Type