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FDA 510(k)

ELIMINATOR AIR FILTER

K-Number: K882468 · 1988-08-29

ApplicantApex Medical, Inc.
Decision Date1988-08-29
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELIMINATOR AIR FILTER 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 1988-08-29 under 510(k) number K882468. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELIMINATOR AIR FILTER?

ELIMINATOR AIR FILTER is a medical device that received FDA 510(k) clearance on 1988-08-29. The listed applicant is Apex Medical, Inc.. The 510(k) number is K882468.

When did ELIMINATOR AIR FILTER receive FDA 510(k) clearance?

ELIMINATOR AIR FILTER received FDA 510(k) clearance on 1988-08-29, under 510(k) number K882468.

Who is the listed applicant for ELIMINATOR AIR FILTER?

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 ELIMINATOR AIR FILTER?

The FDA product code for ELIMINATOR AIR FILTER is KDQ.

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.

K933965APEX MEDICAL AIR PUMPSK902102COM-TENS: A NEUROSTIMULATORK882816PULSAR EMK871570APEX ALPHA VACUUM PUMPK871384APEX SUCTION CURETTE

Related Devices (Code: KDQ)

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.

K081718EXPRESS CHEST DRAINAtrium Medical Corp.K062302MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEMMillicore ABK043582OCEAN CHEST DRAINAtrium Medical Corp.K984496ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAINAtrium Medical Corp.K962856PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTRDeknatel, Inc.K961287ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEMRocket Medical Plc

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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