FDA 510(k)

DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE

K-Number: K850986 · 1985-04-01

Decision Date1985-04-01

Product CodeCEO

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE is the device name listed in this FDA 510(k) record. The listed applicant is Data Medical Associates, Inc.. It received FDA 510(k) clearance on 1985-04-01 under 510(k) number K850986. The device is classified under product code CEO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE?

DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K850986.

When did DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE receive FDA 510(k) clearance?

DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE received FDA 510(k) clearance on 1985-04-01, under 510(k) number K850986.

Who is the listed applicant for DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE?

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

What is the FDA product code for DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE?

The FDA product code for DATE CHEM INORGANIC PHOSPHOROUS U.V. PROCEDURE is CEO.

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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.