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FDA 510(k)

MMI/GAELTEC CATHETER TIP PRESSURE

K-Number: K801755 · 1980-08-13

ApplicantMedical Measurements, Inc.
Decision Date1980-08-13
Product CodeGWM
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MMI/GAELTEC CATHETER TIP PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Measurements, Inc.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801755. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMI/GAELTEC CATHETER TIP PRESSURE?

MMI/GAELTEC CATHETER TIP PRESSURE is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Medical Measurements, Inc.. The 510(k) number is K801755.

When did MMI/GAELTEC CATHETER TIP PRESSURE receive FDA 510(k) clearance?

MMI/GAELTEC CATHETER TIP PRESSURE received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801755.

Who is the listed applicant for MMI/GAELTEC CATHETER TIP PRESSURE?

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

What is the FDA product code for MMI/GAELTEC CATHETER TIP PRESSURE?

The FDA product code for MMI/GAELTEC CATHETER TIP PRESSURE is GWM.

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Other records listing Medical Measurements, 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.

K921062GAELTEC MPR SERIESK902097MODEL TR RECTAL SUCTION BIOPSY TUBEK863479MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURALK801757MMI/GAELTEC CATHETER TIP PRESS. TRANSDUK801756MMI/GAELTEC CATHETER TIP TRANSDUCK801880MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS

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Related Devices (Code: GWM)

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.

K252241Pressio 3 Multi-parameter Neuromonitoring SystemSophysaK250285NEUROVENT-P (092946-003); NEUROVENT (092956-003); NEUROVENT-IFD-R (095317-003); NEUROVENT-IFD-S (091678-003); NEUROVENT-P-TEMP (094268-003); NEUROVENT-TEMP (094278-003); NEUROVENT-TEMP-IFD-R (095327-003); NEUROVENT-TEMP-IFD-S (094288-003); NEUROVENT-PTO (095008-003); NEUROVENT-PTO 2L (095108-003); NEUROVENT-PX (091580-003); BOLT-DRILL KIT CH5 (091888-003); BOLT-DRILL KIT CH9 (091898-003); BOLT-DRILL KIT PTO (092380-003); BOLT-DRILL KIT VP 16 (092969-003); BOLT KIT CH5 (091868-003); BOLRaumedic AGK240821B4C System - Addition of new sensor model (BcSs-PICNIW-2000)Braincare Desenvolvimento E Inovação Tecnológica S.A.K232890CereLink ICP Monitor (826820), CereLink ICP Extension Cable (826845)Integra Lifesciences Production CorporationK201989B4C SystemBraincare Desenvolvimento E Inovacao Tecnologica S.A.K210993CereLink ICP MonitorIntegra Lifesciences Production Corporation

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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