TENCKHOFF PERITONEAL DIALYSIS KIT— 510(k) K902203

Unknown

Akcess Medical Products, Inc.

FDA 510(k) clearance K902203 for TENCKHOFF PERITONEAL DIALYSIS KIT, Unknown on 1990-08-01. Applicant: Akcess Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Akcess Medical Products, Inc.
Product code: Code FJG
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1990-05-16
Decision date: 1990-08-01
Decision: Unknown
Clearance type: Traditional
Location: New Brunswick, 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.