510(k) K870112

STORZ ENT/OPHTHALMIC MAXI CHAIR by Storz Instrument Co. — Product Code HME

K870112 is an FDA 510(k) premarket notification submitted by Storz Instrument Co. for the device "STORZ ENT/OPHTHALMIC MAXI CHAIR". The FDA issued a decision of Substantially Equivalent on February 12, 1987. The device falls under product code HME (Chair, Ophthalmic, Ac-Powered), a Class I device regulated under 21 CFR 886.1140. Storz Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 12, 1987
Date Received
January 12, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Ophthalmic, Ac-Powered
Device Class
Class I
Regulation Number
886.1140
Review Panel
OP
Submission Type