Cleared Traditional

DOBBHOFF(R) RETRIEVAL FORCEPS

K901744 · Biosearch Medical Products, Inc. · Neurology
Jul 1990
Decision
77d
Days
Class 1
Risk

About This 510(k) Submission

K901744 is an FDA 510(k) clearance for the DOBBHOFF(R) RETRIEVAL FORCEPS, a Goniometer, Nonpowered (Class I — General Controls, product code KQW), submitted by Biosearch Medical Products, Inc. (Somerville, US). The FDA issued a Cleared decision on July 3, 1990, 77 days after receiving the submission on April 17, 1990. This device falls under the Neurology review panel. Regulated under 21 CFR 888.1520.

Submission Details

510(k) Number K901744 FDA.gov
FDA Decision Cleared SESE
Date Received April 17, 1990
Decision Date July 03, 1990
Days to Decision 77 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary —

Device Classification

Product Code KQW — Goniometer, Nonpowered
Device Class Class I — General Controls
CFR Regulation 21 CFR 888.1520