Cleared Traditional

K934829 - HASKON MEDICAL GRADE SHEETING

K934829 is an FDA 510(k) clearance for HASKON MEDICAL GRADE SHEETING, manufactured by Haskon Intl., Inc.. The device is a Class 1 General & Plastic Surgery device with product code MDA cleared through the Traditional 510(k) pathway after a 118-day FDA review.

K934829 · Haskon Intl., Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1994
Decision
118d
Days
Class 1
Risk

K934829 is an FDA 510(k) clearance for the HASKON MEDICAL GRADE SHEETING. Classified as Elastomer, Silicone, For Scar Management (product code MDA), Class I - General Controls.

Submitted by Haskon Intl., Inc. (Taunton, US). The FDA issued a Cleared decision on February 3, 1994 after a review of 118 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4025 - 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 Haskon Intl., Inc. devices

FDA 510(k) Submission Details - K934829

510(k) Number K934829 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 08, 1993
Decision Date February 03, 1994
Days to Decision 118 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
3d slower than avg
Panel avg: 115d · This submission: 118d
Pathway characteristics
Predicate-based equivalence.

MDA Device Classification - Class 1, General Controls

Product Code MDA Elastomer, Silicone, For Scar Management
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4025
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 - MDA Elastomer, Silicone, For Scar Management

All 63
Devices cleared under the same product code (MDA) and FDA review panel - the closest regulatory comparables to K934829.
SILK*SKIN SCAR TREATMENT
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NOVAGEL SILICONE GEL SHEETING
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PMT SILICONE SHEETING
K935499 · Pmt Corp. · Feb 1994
CICA-CARE SILICONE GEL SHEET
K935803 · Smith & Nephew United, Inc. · Feb 1994
PMT(R) SILICONE GEL SHEETING MODEL 3505-1
K930409 · Pmt Corp. · Sep 1993
SIL-K
K914701 · Degania Silicone , Ltd. · Jan 1992