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FDA 510(k)

PARATHYROID HORMONE RADIOIMMUNOASSAY KIT

K-Number: K850254 · 1985-04-03

ApplicantCambridge Medical Technology
Decision Date1985-04-03
Product CodeCEW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARATHYROID HORMONE RADIOIMMUNOASSAY KIT 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 1985-04-03 under 510(k) number K850254. The device is classified under product code CEW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARATHYROID HORMONE RADIOIMMUNOASSAY KIT?

PARATHYROID HORMONE RADIOIMMUNOASSAY KIT is a medical device that received FDA 510(k) clearance on 1985-04-03. The listed applicant is Cambridge Medical Technology. The 510(k) number is K850254.

When did PARATHYROID HORMONE RADIOIMMUNOASSAY KIT receive FDA 510(k) clearance?

PARATHYROID HORMONE RADIOIMMUNOASSAY KIT received FDA 510(k) clearance on 1985-04-03, under 510(k) number K850254.

Who is the listed applicant for PARATHYROID HORMONE RADIOIMMUNOASSAY KIT?

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 PARATHYROID HORMONE RADIOIMMUNOASSAY KIT?

The FDA product code for PARATHYROID HORMONE RADIOIMMUNOASSAY KIT is CEW.

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Related Devices (Code: CEW)

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.

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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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