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FDA 510(k)

GASTROGRAPH

K-Number: K903646 · 1990-11-05

ApplicantMedics Instrument Corp.
Decision Date1990-11-05
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GASTROGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Medics Instrument Corp.. It received FDA 510(k) clearance on 1990-11-05 under 510(k) number K903646. 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 GASTROGRAPH?

GASTROGRAPH is a medical device that received FDA 510(k) clearance on 1990-11-05. The listed applicant is Medics Instrument Corp.. The 510(k) number is K903646.

When did GASTROGRAPH receive FDA 510(k) clearance?

GASTROGRAPH received FDA 510(k) clearance on 1990-11-05, under 510(k) number K903646.

Who is the listed applicant for GASTROGRAPH?

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

What is the FDA product code for GASTROGRAPH?

The FDA product code for GASTROGRAPH 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 Medics Instrument 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.

K905154GASTROSCANK821333ATRIAL J TEMPORARY PACING ELECTRODESSK812517CARDIAC PACING ELECTRODES

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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