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FDA 510(k)

ANGIOTENSIN I IMMUTOPE KIT

K-Number: K761267 · 1976-12-30

ApplicantSquibb & Sons, Inc.
Decision Date1976-12-30
Product CodeCIB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANGIOTENSIN I IMMUTOPE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Squibb & Sons, Inc.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K761267. 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 ANGIOTENSIN I IMMUTOPE KIT?

ANGIOTENSIN I IMMUTOPE KIT is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is Squibb & Sons, Inc.. The 510(k) number is K761267.

When did ANGIOTENSIN I IMMUTOPE KIT receive FDA 510(k) clearance?

ANGIOTENSIN I IMMUTOPE KIT received FDA 510(k) clearance on 1976-12-30, under 510(k) number K761267.

Who is the listed applicant for ANGIOTENSIN I IMMUTOPE KIT?

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

What is the FDA product code for ANGIOTENSIN I IMMUTOPE KIT?

The FDA product code for ANGIOTENSIN I IMMUTOPE KIT is CIB.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Squibb & Sons, Inc. as applicant

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.

K821174TSH-SQUIBB RADIOIMMUNOASSAY KITK801424ESTRIOL RIA KIT FOR USE WITH GAMMAFLOK800750STOMAHESIVE STERILE WAFERK770726RIA KIT, T4 CLASP

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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