Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GENERAL PURPOSE COMBINATION PH ELECTRODE

K-Number: K871921 · 1987-10-20

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

Device Summary

GENERAL PURPOSE COMBINATION PH ELECTRODE 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 K871921. 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 GENERAL PURPOSE COMBINATION PH ELECTRODE?

GENERAL PURPOSE COMBINATION PH ELECTRODE 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 K871921.

When did GENERAL PURPOSE COMBINATION PH ELECTRODE receive FDA 510(k) clearance?

GENERAL PURPOSE COMBINATION PH ELECTRODE received FDA 510(k) clearance on 1987-10-20, under 510(k) number K871921.

Who is the listed applicant for GENERAL PURPOSE COMBINATION PH ELECTRODE?

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 GENERAL PURPOSE COMBINATION PH ELECTRODE?

The FDA product code for GENERAL PURPOSE COMBINATION PH ELECTRODE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K873361LIFE-SPAN CABLEK871922PORTABLE PH, MV, TEMP METER W/AUTO. TEMP COMPENSA.

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.

K102543BRAVO PH MONITORING SYSTEM AND ACCESSORIESGiven Imaging , Ltd.K013951SANDHILL SCIENTIFIC PEDIATEC PH PROBESandhill Scientific, Inc.K002028BRAVO PH MONITORING SYSTEMEndonetics, Inc.K961346PH ANALYSIS MODULESynectics-DantecK950087LOT 440Medical Instruments Corporation Mic AGK955018TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATORInstrumentarium Corp.

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.

↑