PERI-BOTTLE— 510(k) K902830

Substantially Equivalent

Orion Life Systems, Inc.

FDA 510(k) clearance K902830 for PERI-BOTTLE, Substantially Equivalent on 1990-08-06. Applicant: Orion Life Systems, Inc.. Device class: 1.

Clearance details

Applicant: Orion Life Systems, Inc.
Product code: Code HED
Device class: Class 1
Regulation: 21 CFR 884.5900
Advisory panel: Obstetrics/Gynecology
Date received: 1990-06-28
Decision date: 1990-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, US

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