SYLVAN PEDIASCAN 200 TRANSILLUMINATOR— 510(k) K901309

Name: FDA 510(k) clearance K901309
Creator: U.S. Food and Drug Administration
Published: 1990-05-24

Substantially Equivalent

Sylvan Corp.

FDA 510(k) clearance K901309 for SYLVAN PEDIASCAN 200 TRANSILLUMINATOR, Substantially Equivalent on 1990-05-24. Applicant: Sylvan Corp.. Device class: 1.

Clearance details

Applicant: Sylvan Corp.
Product code: Code HJN
Device class: Class 1
Regulation: 21 CFR 886.1945
Advisory panel: Ophthalmic
Date received: 1990-03-20
Decision date: 1990-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irwin, PA, US

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K941035 — VENOSCOPE1994-05-16
K912747 — LULMITEX NEONATAL TRANSILLUMINATOR1991-12-24

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