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FDA 510(k)

SWIVEL ADAPTER

K-Number: K900642 · 1990-03-19

ApplicantWilliams Specialty Products, Inc.
Decision Date1990-03-19
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SWIVEL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Williams Specialty Products, Inc.. It received FDA 510(k) clearance on 1990-03-19 under 510(k) number K900642. The device is classified under product code HHI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWIVEL ADAPTER?

SWIVEL ADAPTER is a medical device that received FDA 510(k) clearance on 1990-03-19. The listed applicant is Williams Specialty Products, Inc.. The 510(k) number is K900642.

When did SWIVEL ADAPTER receive FDA 510(k) clearance?

SWIVEL ADAPTER received FDA 510(k) clearance on 1990-03-19, under 510(k) number K900642.

Who is the listed applicant for SWIVEL ADAPTER?

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

What is the FDA product code for SWIVEL ADAPTER?

The FDA product code for SWIVEL ADAPTER is HHI.

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 Williams Specialty Products, 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.

K900641CANNULA, SUCTION UTERINE

Related Devices (Code: HHI)

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.

K171440Berkeley VC-10 Vacuum Curettage SystemGyrus AcmiK030935BERKELEY V-10 VACUUM CURETTAGE SYSTEMAcmi CorporationK983181CYTOPREPCytoprep Inc. Est.K931205MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTERBaxter Healthcare CorpK904160CYTOSMEAR BRUSHBrooke Intl.K900641CANNULA, SUCTION UTERINEWilliams Specialty Products, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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