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FDA 510(k)

ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY

K-Number: K820616 · 1982-03-26

ApplicantE. R. Squibb & Sons, Inc.
Decision Date1982-03-26
Product CodeCIB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is E. R. Squibb & Sons, Inc.. It received FDA 510(k) clearance on 1982-03-26 under 510(k) number K820616. The device is classified under product code CIB. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY?

ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1982-03-26. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K820616.

When did ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY receive FDA 510(k) clearance?

ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY received FDA 510(k) clearance on 1982-03-26, under 510(k) number K820616.

Who is the listed applicant for ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY?

The FDA 510(k) record lists E. R. Squibb & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY?

The FDA product code for ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY is CIB.

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Other records listing E. R. Squibb & Sons, Inc. as applicant

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K821494RIA STAT 16K820340T3 UPTAKE-SQUIBB DIAGNOSTIC KITK820341CORTISOL-SQUIBB RADIOIMMUNOASSAY KITK811240SUR-FIT LOOP OSTOMY O.R. SETK811239SUR-FIT DISPOSABLE CONVEX INSERTK811160SUR-FIT IRRIGATION SLEEVE

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Related Devices (Code: CIB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123763IDS ISYS DIRECT RENIN ASSAY, IDS ISYS DIRECT RENIN CONTROL SET, AND IDS ISYS DIRECT RENIN CALIBRATION VERIFIERSImmunodiagnostic Systems , Ltd.K121944LIAISON DIRECT RENIN LIAISON CONTROL DIRECT RENIN LIAISON ENDOCRINOLOGY DILUENTDiaSorin, Inc.K062120CISBIO RENIN RIA TESTCis Bio InternationalK061758ACTIVE RENIN IRMADiagnostic Systems Laboratories, Inc.K011128NICHOLS ADVANTAGE DIRECT RENIN (CALIBRATORS, CALIBRATION VERIFIERS, CONTROLS, AND SAMPLE DILUENT)Nichols Institute DiagnosticsK981607ACTIVE RENIN IRMA MODEL NUMBER DSL-25100Diagnostic Systems Laboratories, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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