THE TELOS EQUIPMENT— 510(k) K812778

Substantially Equivalent

The Telos Co.

FDA 510(k) clearance K812778 for THE TELOS EQUIPMENT, Substantially Equivalent on 1981-12-08. Applicant: The Telos Co.. Device class: 1.

Clearance details

Applicant: The Telos Co.
Product code: Code KQW
Device class: Class 1
Regulation: 21 CFR 888.1520
Advisory panel: Orthopedic
Date received: 1981-10-05
Decision date: 1981-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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
K870767 — THE (CROM) TESTER1987-03-17
K850082 — HAND HELD GONIOMETER1985-04-04
K831550 — FINGER BONIOMETER BK75061983-06-24

More clearances from The Telos Co.

K812779 — EXTENSIONS-LUSATZTISCH1981-10-26

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