510(k) K831832

H-O CAMERA by Uni-Quatro Industries

K831832 is an FDA 510(k) premarket notification submitted by Uni-Quatro Industries for the device "H-O CAMERA". The FDA issued a decision of Substantially Equivalent on Jul 7, 1983. Uni-Quatro Industries has 2 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Jul 7, 1983
Date Received
Jun 7, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Source: FDA 510(k) database entry for K831832. Report a data issue: hello@regdatalab.com.