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FDA 510(k)

RIA-GNOST INSULIN

K-Number: K890837 · 1989-04-26

ApplicantCambridge Medical Technology
Decision Date1989-04-26
Product CodeCFP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA-GNOST INSULIN is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Medical Technology. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K890837. The device is classified under product code CFP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA-GNOST INSULIN?

RIA-GNOST INSULIN is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Cambridge Medical Technology. The 510(k) number is K890837.

When did RIA-GNOST INSULIN receive FDA 510(k) clearance?

RIA-GNOST INSULIN received FDA 510(k) clearance on 1989-04-26, under 510(k) number K890837.

Who is the listed applicant for RIA-GNOST INSULIN?

The FDA 510(k) record lists Cambridge Medical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA-GNOST INSULIN?

The FDA product code for RIA-GNOST INSULIN is CFP.

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Other records listing Cambridge Medical Technology 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.

K890836RIA-GNOST PROGESTERONEK890697RIA-GNOST FERRITINK873737NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAYK870573T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KITK862871RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOLK860130TESTOSTERONE COATED TUBES RADIOIMMUNOASSAY KIT

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Related Devices (Code: CFP)

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.

K963911ALPCO/MERCODIA INSULIN ELISAAmerican Laboratory Products Co., Ltd.K953084ACCESS ULTRASENSITIVE INSULIN ASSAYBio-Rad Laboratories, Inc.K920109IMX INSULINAbbott LaboratoriesK914820DSL INSULIN RIA (DSL 1600)Diagnostic Systems Laboratories, Inc.K903628AIA-PACK IRITosoh Corp.K901135ENZYMUN TEST(R) INSULINBoehringer Mannheim Corp.

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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