PERMA PURE NAFION TUBE DRYER-MODEL ME— 510(k) K881264

Name: FDA 510(k) clearance K881264
Creator: U.S. Food and Drug Administration
Published: 1988-10-25

Substantially Equivalent

Perma Pure Products, Inc.

FDA 510(k) clearance K881264 for PERMA PURE NAFION TUBE DRYER-MODEL ME, Substantially Equivalent on 1988-10-25. Applicant: Perma Pure Products, Inc.. Device class: 2.

Clearance details

Applicant: Perma Pure Products, Inc.
Product code: Code CBQ
Device class: Class 2
Regulation: 21 CFR 868.1500
Advisory panel: Anesthesiology
Date received: 1988-03-24
Decision date: 1988-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toms River, NJ, US

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