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FDA 510(k)

APEX MEDICAL AIR PUMPS

K-Number: K933965 · 1994-03-17

ApplicantApex Medical, Inc.
Decision Date1994-03-17
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

APEX MEDICAL AIR PUMPS is the device name listed in this FDA 510(k) record. The listed applicant is Apex Medical, Inc.. It received FDA 510(k) clearance on 1994-03-17 under 510(k) number K933965. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX MEDICAL AIR PUMPS?

APEX MEDICAL AIR PUMPS is a medical device that received FDA 510(k) clearance on 1994-03-17. The listed applicant is Apex Medical, Inc.. The 510(k) number is K933965.

When did APEX MEDICAL AIR PUMPS receive FDA 510(k) clearance?

APEX MEDICAL AIR PUMPS received FDA 510(k) clearance on 1994-03-17, under 510(k) number K933965.

Who is the listed applicant for APEX MEDICAL AIR PUMPS?

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

What is the FDA product code for APEX MEDICAL AIR PUMPS?

The FDA product code for APEX MEDICAL AIR PUMPS is FNM.

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 Apex Medical, 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.

K902102COM-TENS: A NEUROSTIMULATORK882816PULSAR EMK882468ELIMINATOR AIR FILTERK871570APEX ALPHA VACUUM PUMPK871384APEX SUCTION CURETTE

Related Devices (Code: FNM)

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.

K973169PRESSURE GUARD SITE SELECT (A)Span-America Medical Systems, Inc.K972022ZAK-2000Cardio Systems, Inc.K974319MIGHTY AIRWheelchairs of KansasK974070PHYSIO/1000Physio Designs, Inc.K972549SIMPULSEKinetic Concepts, Inc.K970081SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEMCathay Consolidated, Inc.

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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