MERCY HIP/KNEE PACK— 510(k) K896215

Name: FDA 510(k) clearance K896215
Creator: U.S. Food and Drug Administration
Published: 1990-02-13

Substantially Equivalent

Westmark, Sterile Packing Systems, Inc. (Sps)

FDA 510(k) clearance K896215 for MERCY HIP/KNEE PACK, Substantially Equivalent on 1990-02-13. Applicant: Westmark, Sterile Packing Systems, Inc. (Sps). Device class: 2.

Clearance details

Applicant: Westmark, Sterile Packing Systems, Inc. (Sps)
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1989-10-26
Decision date: 1990-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

Download summary PDF View on FDA.gov ↗

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K896800 — IRRIGATION TRAY1990-05-24
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K896559 — INFANT FEEDING TUBE1990-03-13
K896794 — SPECIMEN CONTAINER1990-03-01
K896806 — CATHETER PLUG/PROTECTOR1990-02-26

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