INTRAY GC— 510(k) K993033

Substantially Equivalent

Biomed Diagnostics, Inc.

FDA 510(k) clearance K993033 for INTRAY GC, Substantially Equivalent on 1999-12-16. Applicant: Biomed Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Biomed Diagnostics, Inc.
Product code: Code JTY
Device class: Class 2
Regulation: 21 CFR 866.2410
Advisory panel: Microbiology
Date received: 1999-09-09
Decision date: 1999-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

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