FDA 510(k)

INORGANIC PHOSPHORUS REAGENTS

K-Number: K811222 · 1981-05-21

Decision Date1981-05-21

Product CodeCED

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

INORGANIC PHOSPHORUS REAGENTS is the device name listed in this FDA 510(k) record. The listed applicant is Connecticut Diagnostics, Ltd.. It received FDA 510(k) clearance on 1981-05-21 under 510(k) number K811222. The device is classified under product code CED. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INORGANIC PHOSPHORUS REAGENTS?

INORGANIC PHOSPHORUS REAGENTS is a medical device that received FDA 510(k) clearance on 1981-05-21. The listed applicant is Connecticut Diagnostics, Ltd.. The 510(k) number is K811222.

When did INORGANIC PHOSPHORUS REAGENTS receive FDA 510(k) clearance?

INORGANIC PHOSPHORUS REAGENTS received FDA 510(k) clearance on 1981-05-21, under 510(k) number K811222.

Who is the listed applicant for INORGANIC PHOSPHORUS REAGENTS?

The FDA 510(k) record lists Connecticut Diagnostics, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INORGANIC PHOSPHORUS REAGENTS?

The FDA product code for INORGANIC PHOSPHORUS REAGENTS is CED.

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Other records listing Connecticut Diagnostics, Ltd. as applicant

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Related Devices (Code: CED)

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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.