DYNAMIC CRUCIATE TESTER— 510(k) K881876

Substantially Equivalent

Dyonics, Inc.

FDA 510(k) clearance K881876 for DYNAMIC CRUCIATE TESTER, Substantially Equivalent on 1988-11-17. Applicant: Dyonics, Inc.. Device class: 1.

Clearance details

Applicant: Dyonics, Inc.
Product code: Code LYH
Device class: Class 1
Regulation: 21 CFR 890.1615
Advisory panel: Physical Medicine
Date received: 1988-05-04
Decision date: 1988-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LYH

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K942059 — KT2000 KNEE LIGAMENT ARTHROMETER1994-09-20
K834462 — GENUCOM1984-02-09
K812806 — KT-1000 DEVICE1981-11-10

More clearances from Dyonics, Inc.

K900070 — MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM1990-02-16
K896416 — DYONICS SHOULDER PORTAL SYSTEM1990-01-02
K893136 — SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTY1989-12-14
K890665 — MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES1989-11-03
K894728 — DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFE1989-08-18

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