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FDA 510(k)

APEX SUCTION CURETTE

K-Number: K871384 · 1987-05-22

ApplicantApex Medical, Inc.
Decision Date1987-05-22
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

APEX SUCTION CURETTE 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 1987-05-22 under 510(k) number K871384. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX SUCTION CURETTE?

APEX SUCTION CURETTE is a medical device that received FDA 510(k) clearance on 1987-05-22. The listed applicant is Apex Medical, Inc.. The 510(k) number is K871384.

When did APEX SUCTION CURETTE receive FDA 510(k) clearance?

APEX SUCTION CURETTE received FDA 510(k) clearance on 1987-05-22, under 510(k) number K871384.

Who is the listed applicant for APEX SUCTION CURETTE?

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 SUCTION CURETTE?

The FDA product code for APEX SUCTION CURETTE is GEA.

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 EMK882468ELIMINATOR AIR FILTERK871570APEX ALPHA VACUUM PUMP

Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, 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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