510(k) K801638
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