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FDA 510(k)

MODEL SA3 ESOPHAGEAL PH ELECTRODE

K-Number: K852289 · 1985-07-25

ApplicantWorld Precision Instruments, Inc.
Decision Date1985-07-25
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL SA3 ESOPHAGEAL PH ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is World Precision Instruments, Inc.. It received FDA 510(k) clearance on 1985-07-25 under 510(k) number K852289. 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 MODEL SA3 ESOPHAGEAL PH ELECTRODE?

MODEL SA3 ESOPHAGEAL PH ELECTRODE is a medical device that received FDA 510(k) clearance on 1985-07-25. The listed applicant is World Precision Instruments, Inc.. The 510(k) number is K852289.

When did MODEL SA3 ESOPHAGEAL PH ELECTRODE receive FDA 510(k) clearance?

MODEL SA3 ESOPHAGEAL PH ELECTRODE received FDA 510(k) clearance on 1985-07-25, under 510(k) number K852289.

Who is the listed applicant for MODEL SA3 ESOPHAGEAL PH ELECTRODE?

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

What is the FDA product code for MODEL SA3 ESOPHAGEAL PH ELECTRODE?

The FDA product code for MODEL SA3 ESOPHAGEAL 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.

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Other records listing World Precision Instruments, Inc. 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.

K883869DERMTRODE

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.

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