ORION STERILE OR TOWELS— 510(k) K903117

Name: FDA 510(k) clearance K903117
Creator: U.S. Food and Drug Administration
Published: 1990-12-31

Substantially Equivalent

Orion Life Systems, Inc.

FDA 510(k) clearance K903117 for ORION STERILE OR TOWELS, Substantially Equivalent on 1990-12-31. Applicant: Orion Life Systems, Inc.. Device class: 2.

Clearance details

Applicant: Orion Life Systems, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1990-07-16
Decision date: 1990-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, US

Download summary PDF View on FDA.gov ↗

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K943835 — PRE-FILLED SYRINGE W/STERILE .25% ACETC ACID1995-01-24
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K943829 — PRE-FILLED SYSRINGE W/STERILE WATER1994-11-21
K943830 — PRE-FILLED SYRINGE W/STERILE 0.9% SODIUM CHLORIDE SOLUTION1994-11-21
K943831 — PRE-FILLED 30CC INFLATION SYRINGE W/STERILE WATER1994-11-21

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