NASP TRANSPARENT DRESSING— 510(k) K963753

Name: FDA 510(k) clearance K963753
Creator: U.S. Food and Drug Administration
Published: 1996-11-29

Substantially Equivalent

North American Sterilization & Packaging Co.

FDA 510(k) clearance K963753 for NASP TRANSPARENT DRESSING, Substantially Equivalent on 1996-11-29. Applicant: North American Sterilization & Packaging Co.. Device class: Unclassified.

Clearance details

Applicant: North American Sterilization & Packaging Co.
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 1996-09-18
Decision date: 1996-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparta, NJ, US

Download summary PDF View on FDA.gov ↗

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K991214 — SIMPLICARE TRANSPARENT WOUND DRESSING1999-10-14

More clearances from North American Sterilization & Packaging Co.

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K964231 — NASP HYDROCOLLOID DRESSING (REGULAR OR THIN)1997-03-10
K962352 — HYDROGEL SKIN DRESSING1996-08-02
K925588 — NORTEC STER SALINE-O.9% SODIUM CHLOR FOR DEV IRRI1993-12-03
K925593 — NORTEC STERILE WATER FOR DEVICE IRRIGATION1993-12-03
K925161 — NORTEC STERILE WATER FOR CATHETER BALLOON INFLATIO1993-07-21

Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

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.