Cleared Traditional

ADLER CUSTOM PROCEDURE PACKS (K841723) - FDA 510(k) Clearance

K841723 · Adler Instrument Co. · General & Plastic Surgery device
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Aug 1984
Decision
98d
Days
-
Risk

K841723 is an FDA 510(k) clearance for the ADLER CUSTOM PROCEDURE PACKS.

Submitted by Adler Instrument Co. (Mchenry, US). The FDA issued a Cleared decision on August 1, 1984 after a review of 98 days - within the typical 510(k) review window.

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

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Submission Details

510(k) Number K841723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1984
Decision Date August 01, 1984
Days to Decision 98 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
17d faster than avg
Panel avg: 115d · This submission: 98d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -