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FDA 510(k)

MATCHED COMPONENT SET FOR DIGITOXIN

K-Number: K834080 · 1984-02-04

ApplicantCambridge Medical Technology
Decision Date1984-02-04
Product CodeLCW
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MATCHED COMPONENT SET FOR DIGITOXIN 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 1984-02-04 under 510(k) number K834080. The device is classified under product code LCW. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATCHED COMPONENT SET FOR DIGITOXIN?

MATCHED COMPONENT SET FOR DIGITOXIN is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Cambridge Medical Technology. The 510(k) number is K834080.

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

MATCHED COMPONENT SET FOR DIGITOXIN received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834080.

Who is the listed applicant for MATCHED COMPONENT SET FOR DIGITOXIN?

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 DIGITOXIN?

The FDA product code for MATCHED COMPONENT SET FOR DIGITOXIN is LCW.

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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: LCW)

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.

K802461ENDAB DIGITOXIN ENZYME IMMUNOASSAY KITImmunotech Corp.K780766(125 I) DIGITOXIN RIA KITDiagnostic Products 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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