SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)— 510(k) K963570

Name: FDA 510(k) clearance K963570
Creator: U.S. Food and Drug Administration
Published: 1996-10-18

Substantially Equivalent

Smiths Industries Medical Systems, Inc.

FDA 510(k) clearance K963570 for SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22), Substantially Equivalent on 1996-10-18. Applicant: Smiths Industries Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Smiths Industries Medical Systems, Inc.
Product code: Code FMJ
Device class: Class 2
Regulation: 21 CFR 880.2500
Advisory panel: General Hospital
Date received: 1996-09-05
Decision date: 1996-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Keene, NH, US

Download summary PDF View on FDA.gov ↗

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