510(k) K801638

A O CUSTOM II CHAIR AND STAND by American Optical Corp. — Product Code HME

K801638 is an FDA 510(k) premarket notification submitted by American Optical Corp. for the device "A O CUSTOM II CHAIR AND STAND". The FDA issued a decision of Substantially Equivalent on August 13, 1980. The device falls under product code HME (Chair, Ophthalmic, Ac-Powered), a Class I device regulated under 21 CFR 886.1140. American Optical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 13, 1980
Date Received
July 17, 1980
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