Cleared Traditional

K963753 - NASP TRANSPARENT DRESSING
(FDA 510(k) Clearance)

Nov 1996
Decision
72d
Days
Risk

K963753 is an FDA 510(k) clearance for the NASP TRANSPARENT DRESSING. This device is classified as a Dressing, Wound And Burn, Occlusive.

Submitted by North American Sterilization & Packaging Co. (Sparta, US). The FDA issued a Cleared decision on November 29, 1996, 72 days after receiving the submission on September 18, 1996.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number K963753 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 18, 1996
Decision Date November 29, 1996
Days to Decision 72 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement

Device Classification

Product Code MGP — Dressing, Wound And Burn, Occlusive
Device Class

Similar Devices — MGP Dressing, Wound And Burn, Occlusive

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