Arch Development Group

Arch Development Group holds 2 FDA 510(k) medical device clearances, cleared in 1991.

Top product codes for Arch Development Group

KKX — General, Plastic Surgery1 device
MHW — General Hospital1 device

Recent clearances by Arch Development Group

K913047 — STERILESERT(TM) CABLE AND POLE DRAPECode KKX·1991-10-02
K912765 — STASIS BUTTON PRSSURE DEVICECode MHW·1991-08-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.