MASTER KIT B— 510(k) K861142

Unknown

Pro-Lab, Inc.

FDA 510(k) clearance K861142 for MASTER KIT B, Unknown on 1986-07-10. Applicant: Pro-Lab, Inc.. Device class: 1.

Clearance details

Applicant: Pro-Lab, Inc.
Product code: Code LRP
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1986-03-26
Decision date: 1986-07-10
Decision: Unknown
Clearance type: Traditional
Location: Birmingham, AL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Pro-Lab, Inc.

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K903714 — E. COLI 0157 LATEX TEST1991-01-24
K894221 — ROSCO PYRR1989-09-28

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