Cleared Traditional

VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560 (K924835) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K924835 · American Healthcare Supply Co., Inc. · General & Plastic Surgery device
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Mar 1993
Decision
179d
Days
Class 1
Risk

K924835 is an FDA 510(k) clearance for the VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560. Classified as Suture Removal Kit (product code MCZ), Class I - General Controls.

Submitted by American Healthcare Supply Co., Inc. (South Plainfield, US). The FDA issued a Cleared decision on March 23, 1993 after a review of 179 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - 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 American Healthcare Supply Co., Inc. devices

Submission Details

510(k) Number K924835 FDA.gov
FDA Decision Cleared Substantially Equivalent - Special 510(k) (SESK)
Date Received September 25, 1992
Decision Date March 23, 1993
Days to Decision 179 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
64d slower than avg
Panel avg: 115d · This submission: 179d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code MCZ Suture Removal Kit
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
Definition This Product Code Has Been Established In Accordance With The May 20, 1997, Guidance Entitled, Convenience Kits Interim Regulatory Guidance, Found At Http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm080217.pdf. This Type Of Convenience Kit, As Listed In The Guidance Above, Is Under Enforcement Discretion, And Does Not Require A Premarket Notification (510(k)) To Market If It Meets All Criteria In The Guidance.
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.