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FDA 510(k)

PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA.

K-Number: K871922 · 1987-10-20

ApplicantChemfet Corp.
Decision Date1987-10-20
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA. is the device name listed in this FDA 510(k) record. The listed applicant is Chemfet Corp.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K871922. The device is classified under product code FFT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA.?

PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA. is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Chemfet Corp.. The 510(k) number is K871922.

When did PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA. receive FDA 510(k) clearance?

PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA. received FDA 510(k) clearance on 1987-10-20, under 510(k) number K871922.

Who is the listed applicant for PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA.?

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

What is the FDA product code for PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA.?

The FDA product code for PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA. is FFT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Chemfet Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FFT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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