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FDA 510(k)

IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN

K-Number: K852441 · 1985-08-21

ApplicantClinical Data, Inc.
Decision Date1985-08-21
Product CodeCJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Data, Inc.. It received FDA 510(k) clearance on 1985-08-21 under 510(k) number K852441. The device is classified under product code CJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN?

IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN is a medical device that received FDA 510(k) clearance on 1985-08-21. The listed applicant is Clinical Data, Inc.. The 510(k) number is K852441.

When did IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN receive FDA 510(k) clearance?

IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN received FDA 510(k) clearance on 1985-08-21, under 510(k) number K852441.

Who is the listed applicant for IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN?

The FDA 510(k) record lists Clinical Data, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN?

The FDA product code for IN VITRO TESTS FOR PHOSPHATASE & BLOOD NITROGEN is CJE.

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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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