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FDA 510(k)

MATCHED COMPONENT SET FOR RADIOIMMUNO-

K-Number: K843635 · 1984-09-28

ApplicantCambridge Medical Technology
Decision Date1984-09-28
Product CodeJKC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MATCHED COMPONENT SET FOR RADIOIMMUNO- 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 1984-09-28 under 510(k) number K843635. The device is classified under product code JKC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATCHED COMPONENT SET FOR RADIOIMMUNO-?

MATCHED COMPONENT SET FOR RADIOIMMUNO- is a medical device that received FDA 510(k) clearance on 1984-09-28. The listed applicant is Cambridge Medical Technology. The 510(k) number is K843635.

When did MATCHED COMPONENT SET FOR RADIOIMMUNO- receive FDA 510(k) clearance?

MATCHED COMPONENT SET FOR RADIOIMMUNO- received FDA 510(k) clearance on 1984-09-28, under 510(k) number K843635.

Who is the listed applicant for MATCHED COMPONENT SET FOR RADIOIMMUNO-?

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 MATCHED COMPONENT SET FOR RADIOIMMUNO-?

The FDA product code for MATCHED COMPONENT SET FOR RADIOIMMUNO- is JKC.

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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 INSULINK890836RIA-GNOST PROGESTERONEK890697RIA-GNOST FERRITINK873737NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAYK870573T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KITK862871RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOL

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Related Devices (Code: JKC)

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.

K040181ACCESS DHEA-S REAGENT ASSAYBeckman Coulter, Inc.K003174ELECSYS DHEA-SRoche Diagnostics Corp.K973897DHEA-SKmi Diagnostics, Inc.K962895DSL DHEA-S-7Diagnostic Systems Laboratories, Inc.K955114DSL AACTIVE DHEA EIA KITDiagnostic Systems Laboratories, Inc.K950524NICHOLS INSTITUTE DIAGNOSTICS DHEA-S CHEMILUMINESCENCE IMMUNOASSAYNichols Institute

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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