O'BRIEN GONIOMETER— 510(k) K926237

Substantially Equivalent

Sgarlato Laboratories, Inc.

FDA 510(k) clearance K926237 for O'BRIEN GONIOMETER, Substantially Equivalent on 1993-08-02. Applicant: Sgarlato Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Sgarlato Laboratories, Inc.
Product code: Code KQW
Device class: Class 1
Regulation: 21 CFR 888.1520
Advisory panel: Orthopedic
Date received: 1992-12-11
Decision date: 1993-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQW

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K831550 — FINGER BONIOMETER BK75061983-06-24
K812778 — THE TELOS EQUIPMENT1981-12-08

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