STEAMLINE— 510(k) K895910

Substantially Equivalent

Propper Mfg. Co., Inc.

FDA 510(k) clearance K895910 for STEAMLINE, Substantially Equivalent on 1990-08-22. Applicant: Propper Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Mfg. Co., Inc.
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1989-10-10
Decision date: 1990-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island City, NY, 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.