510(k) K884630

MULTI-PURPOSE HOLDER by Med-Dex Intl. — Product Code LDQ

K884630 is an FDA 510(k) premarket notification submitted by Med-Dex Intl. for the device "MULTI-PURPOSE HOLDER". The FDA issued a decision of Substantially Equivalent on Nov 22, 1988. Med-Dex Intl. has 3 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Nov 22, 1988
Date Received
Nov 7, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Source: FDA 510(k) database entry for K884630. Report a data issue: hello@regdatalab.com.