CLOSED WOUND RESERVOIR— 510(k) K896803

Name: FDA 510(k) clearance K896803
Creator: U.S. Food and Drug Administration
Published: 1989-12-27

Substantially Equivalent

Westmark, Sterile Packing Systems, Inc. (Sps)

FDA 510(k) clearance K896803 for CLOSED WOUND RESERVOIR, Substantially Equivalent on 1989-12-27. Applicant: Westmark, Sterile Packing Systems, Inc. (Sps). Device class: 1.

Clearance details

Applicant: Westmark, Sterile Packing Systems, Inc. (Sps)
Product code: Code GCY
Device class: Class 1
Regulation: 21 CFR 878.4680
Advisory panel: General, Plastic Surgery
Date received: 1989-12-01
Decision date: 1989-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GCY

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K972703 — REDYROB-CLOSED WOUND DRAINAGE SYSTEM1997-10-01
K971036 — ODONTIT AUTOGENOUS BONE COLLECTION DEVICE1997-06-03
K963839 — CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-5001996-12-12
K960099 — PENROSE DRAIN MODELS 6001 - 60071996-03-11
K950754 — MACRO SUCTION TUBE MODEL NO 100611995-04-25

More clearances from Westmark, Sterile Packing Systems, Inc. (Sps)

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K896800 — IRRIGATION TRAY1990-05-24
K896799 — PARACERVICAL/PUDENDAL TRAYS1990-04-23
K896559 — INFANT FEEDING TUBE1990-03-13
K896794 — SPECIMEN CONTAINER1990-03-01
K896806 — CATHETER PLUG/PROTECTOR1990-02-26

Adverse events under product code GCY

product code GCY

Malfunction: 786
Other: 1
Total: 787

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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