510(k) K820636
K820636 is an FDA 510(k) premarket notification submitted by Storz Instrument Co. for the device "STORZ #6500 POWER EXAMINATION CHAIR". The FDA issued a decision of Substantially Equivalent on March 26, 1982. The device falls under product code GBB (Chair, Surgical, Ac-Powered), a Class I device regulated under 21 CFR 878.4960. Storz Instrument Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 26, 1982
- Date Received
- March 8, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chair, Surgical, Ac-Powered
- Device Class
- Class I
- Regulation Number
- 878.4960
- Review Panel
- SU
- Submission Type