Cleared Traditional

K833777 - ANGIOTENSIN CONVERTING ENZYME

K833777 is the FDA 510(k) clearance for ANGIOTENSIN CONVERTING ENZYME by Immuno-Diagnostic Laboratories. It is a Class 2 Chemistry device (product code CIB) cleared through the Traditional 510(k) pathway after a 95-day FDA review.

K833777 · Immuno-Diagnostic Laboratories · Chemistry device
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Jan 1984
Decision
95d
Days
Class 2
Risk

K833777 is an FDA 510(k) clearance for the ANGIOTENSIN CONVERTING ENZYME. Classified as Radioimmunoassay, Angiotensin I And Renin (product code CIB), Class II - Special Controls.

Submitted by Immuno-Diagnostic Laboratories (Mchenry, US). The FDA issued a Cleared decision on January 30, 1984 after a review of 95 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1085 - the FDA in vitro diagnostics and chemistry 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 Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Immuno-Diagnostic Laboratories devices

Submission Details

510(k) Number K833777 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 27, 1983
Decision Date January 30, 1984
Days to Decision 95 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
7d slower than avg
Panel avg: 88d · This submission: 95d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CIB Radioimmunoassay, Angiotensin I And Renin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1085
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CIB Radioimmunoassay, Angiotensin I And Renin

All 8
Devices cleared under the same product code (CIB) and FDA review panel - the closest regulatory comparables to K833777.
ACTIVE RENIN IRMA MODEL NUMBER DSL-25100
K981607 · Diagnostic Systems Laboratories, Inc. · May 1998
ACTIVE RENIN IMMUNORADIOMETRIC ASSAY
K925998 · Nichols Institute Diagnostics · Jan 1993
RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI
K850054 · E.I. Dupont DE Nemours & Co., Inc. · Mar 1985
RENAK
K831694 · Hoffmann-La Roche, Inc. · Jul 1983
ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY
K820616 · E. R. Squibb & Sons, Inc. · Mar 1982