INTRA-ARTICULAR SURGICAL SYSTEM— 510(k) K820367

Substantially Equivalent

Dyonics, Inc.

FDA 510(k) clearance K820367 for INTRA-ARTICULAR SURGICAL SYSTEM, Substantially Equivalent on 1982-05-07. Applicant: Dyonics, Inc.. Device class: 1.

Clearance details

Applicant: Dyonics, Inc.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1982-02-09
Decision date: 1982-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Dyonics, Inc.

K900070 — MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM1990-02-16
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K890665 — MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES1989-11-03
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Data sourced from openFDA. This site is unofficial and independent of the FDA.