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FDA 510(k)

MICROSPAN -PH MONITOR

K-Number: K842303 · 1984-10-12

ApplicantBiochem International, Inc.
Decision Date1984-10-12
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICROSPAN -PH MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Biochem International, Inc.. It received FDA 510(k) clearance on 1984-10-12 under 510(k) number K842303. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSPAN -PH MONITOR?

MICROSPAN -PH MONITOR is a medical device that received FDA 510(k) clearance on 1984-10-12. The listed applicant is Biochem International, Inc.. The 510(k) number is K842303.

When did MICROSPAN -PH MONITOR receive FDA 510(k) clearance?

MICROSPAN -PH MONITOR received FDA 510(k) clearance on 1984-10-12, under 510(k) number K842303.

Who is the listed applicant for MICROSPAN -PH MONITOR?

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

What is the FDA product code for MICROSPAN -PH MONITOR?

The FDA product code for MICROSPAN -PH MONITOR is CBF.

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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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