Cleared Traditional

PAN-PRA AID SELF-ADHE. COLLO. COATED BANDAGE (K881426) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K881426 · Laboratoire Pan-Pra · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1988
Decision
219d
Days
Class 1
Risk

K881426 is an FDA 510(k) clearance for the PAN-PRA AID SELF-ADHE. COLLO. COATED BANDAGE. Classified as Dressing, Wound, Occlusive (product code NAD), Class I - General Controls.

Submitted by Laboratoire Pan-Pra (Canada, CA). The FDA issued a Cleared decision on November 10, 1988 after a review of 219 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4020 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Laboratoire Pan-Pra devices

Submission Details

510(k) Number K881426 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received April 05, 1988
Decision Date November 10, 1988
Days to Decision 219 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
104d slower than avg
Panel avg: 115d · This submission: 219d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code NAD Dressing, Wound, Occlusive
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4020
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - NAD Dressing, Wound, Occlusive

All 11
Devices cleared under the same product code (NAD) and FDA review panel - the closest regulatory comparables to K881426.
MEDLINE STERILE GAUZE SPONGES
K930697 · Medline Industries, Inc. · Jun 1993
TEGAPORE WOUND CONTACT MATERIAL, PRODUCT #563X
K890354 · 3M Company · Apr 1989
3M WOUND CONTACT MATERIAL, PRODUCT #563X
K881988 · 3M Company · Jun 1988
PHARMACLUSIVE (TM)
K872573 · Pharmacia, Inc. · Feb 1988
TRANSIGEN EXUDATE CONTROLLED WOUND DRESSING
K872988 · Smith & Nephew, Inc. · Sep 1987
STRETCH GAUZE BANDAGES
K872875 · Abco Dealers, Inc. · Sep 1987