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FDA 510(k)

NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY

K-Number: K873737 · 1987-11-24

ApplicantCambridge Medical Technology
Decision Date1987-11-24
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY 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 1987-11-24 under 510(k) number K873737. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY?

NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1987-11-24. The listed applicant is Cambridge Medical Technology. The 510(k) number is K873737.

When did NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY receive FDA 510(k) clearance?

NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY received FDA 510(k) clearance on 1987-11-24, under 510(k) number K873737.

Who is the listed applicant for NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY?

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 NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY?

The FDA product code for NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY is CDP.

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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.

K890837RIA-GNOST INSULINK890697RIA-GNOST FERRITINK890836RIA-GNOST PROGESTERONEK870573T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KITK862871RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOLK860130TESTOSTERONE COATED TUBES RADIOIMMUNOASSAY KIT

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Related Devices (Code: CDP)

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.

K001607REPROBEAD T3 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 104)Repromedix Corp.K991692CHIRON DIAGNOSTICS ACS: 180 FT3Chiron Diagnostics Corp.K991311TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005Biocheck, Inc.K991252AIA-PACK FT3 ASSAYTosoh Medics, Inc.K981824OPTICOAT T3 EIA KITBiotecx Laboratories, Inc.K983439ABBOTT ARCHITECT FREE T3Abbott Laboratories

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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