THE (CROM) TESTER— 510(k) K870767

Substantially Equivalent

Twin City Surgical, Inc.

FDA 510(k) clearance K870767 for THE (CROM) TESTER, Substantially Equivalent on 1987-03-17. Applicant: Twin City Surgical, Inc.. Device class: 1.

Clearance details

Applicant: Twin City Surgical, Inc.
Product code: Code KQW
Device class: Class 1
Regulation: 21 CFR 888.1520
Advisory panel: Orthopedic
Date received: 1987-02-26
Decision date: 1987-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQW

K926237 — O'BRIEN GONIOMETER1993-08-02
K901744 — DOBBHOFF(R) RETRIEVAL FORCEPS1990-07-03
K850082 — HAND HELD GONIOMETER1985-04-04
K831550 — FINGER BONIOMETER BK75061983-06-24
K812778 — THE TELOS EQUIPMENT1981-12-08

More clearances from Twin City Surgical, Inc.

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