Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONTAIN(TM)

K-Number: K874505 · 1988-05-20

ApplicantArbor Technologies, Inc.
Decision Date1988-05-20
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONTAIN(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Arbor Technologies, Inc.. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K874505. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTAIN(TM)?

CONTAIN(TM) is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K874505.

When did CONTAIN(TM) receive FDA 510(k) clearance?

CONTAIN(TM) received FDA 510(k) clearance on 1988-05-20, under 510(k) number K874505.

Who is the listed applicant for CONTAIN(TM)?

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

What is the FDA product code for CONTAIN(TM)?

The FDA product code for CONTAIN(TM) is GCX.

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 Arbor Technologies, 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.

K960928SYRINGEFILTERK964283AUTOPRIMEK922777PRESSURE TUBING AND ACCESSORIESK902666ANESTHESIA CONDUCTION FILTERK895859CONTAIN(TM)K902167CONTAIN(TM) LASER PLUME FILTER

View all 10 devices →

Related Devices (Code: GCX)

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.

K042454STRYKER CASSETTE PUMPStryker EndoscopyK992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMCircon Corp.K972074SUCTION INSTRUMENTATIONWalter Lorenz Surgical, Inc.K971022CHASE SUCKERChase Medical, Inc.K964127MEDI-VAC FLEXI-CLEAR SUCTION HANDLEAllegiance Healthcare Corp.K964519CURITY THORACENTESIS TRAYKendall Healthcare Products Co. Div.Of Tyco Health

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.

↑