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FDA 510(k)

CANNULA, SUCTION UTERINE

K-Number: K900641 · 1990-03-30

ApplicantWilliams Specialty Products, Inc.
Decision Date1990-03-30
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CANNULA, SUCTION UTERINE 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 1990-03-30 under 510(k) number K900641. 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 CANNULA, SUCTION UTERINE?

CANNULA, SUCTION UTERINE is a medical device that received FDA 510(k) clearance on 1990-03-30. The listed applicant is Williams Specialty Products, Inc.. The 510(k) number is K900641.

When did CANNULA, SUCTION UTERINE receive FDA 510(k) clearance?

CANNULA, SUCTION UTERINE received FDA 510(k) clearance on 1990-03-30, under 510(k) number K900641.

Who is the listed applicant for CANNULA, SUCTION UTERINE?

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 CANNULA, SUCTION UTERINE?

The FDA product code for CANNULA, SUCTION UTERINE 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.

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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.

K900642SWIVEL ADAPTER

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.K900642SWIVEL ADAPTERWilliams 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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