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FDA 510(k)

PARATHYROID HORMONE MID-MOLECULE RIA-KIT

K-Number: K843870 · 1984-10-30

ApplicantDiagnostic Products Corp.
Decision Date1984-10-30
Product CodeCEW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARATHYROID HORMONE MID-MOLECULE RIA-KIT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1984-10-30 under 510(k) number K843870. 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 MID-MOLECULE RIA-KIT?

PARATHYROID HORMONE MID-MOLECULE RIA-KIT is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K843870.

When did PARATHYROID HORMONE MID-MOLECULE RIA-KIT receive FDA 510(k) clearance?

PARATHYROID HORMONE MID-MOLECULE RIA-KIT received FDA 510(k) clearance on 1984-10-30, under 510(k) number K843870.

Who is the listed applicant for PARATHYROID HORMONE MID-MOLECULE RIA-KIT?

The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARATHYROID HORMONE MID-MOLECULE RIA-KIT?

The FDA product code for PARATHYROID HORMONE MID-MOLECULE RIA-KIT is CEW.

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Related Devices (Code: CEW)

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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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