AQUALUBE(TM)— 510(k) K864556

Substantially Equivalent

Parker Laboratories, Inc.

FDA 510(k) clearance K864556 for AQUALUBE(TM), Substantially Equivalent on 1986-12-01. Applicant: Parker Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Parker Laboratories, Inc.
Product code: Code KMJ
Device class: Class 1
Regulation: 21 CFR 880.6375
Advisory panel: General Hospital
Date received: 1986-11-19
Decision date: 1986-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange, NJ, US

Download summary PDF View on FDA.gov ↗

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