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FDA 510(k)

CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE

K-Number: K875084 · 1988-02-08

ApplicantCabot Medical Corp.
Decision Date1988-02-08
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1988-02-08 under 510(k) number K875084. The device is classified under product code HHK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE?

CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE is a medical device that received FDA 510(k) clearance on 1988-02-08. The listed applicant is Cabot Medical Corp.. The 510(k) number is K875084.

When did CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE receive FDA 510(k) clearance?

CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE received FDA 510(k) clearance on 1988-02-08, under 510(k) number K875084.

Who is the listed applicant for CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE?

The FDA 510(k) record lists Cabot Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE?

The FDA product code for CABOT MEDICAL ENDOMETRIAL SUCTION CURETTE is HHK.

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Other records listing Cabot Medical Corp. 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.

K960148CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENTK946109CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPSK951972CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHSK951714CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBERK941743CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMPK9341153000 ELECTRONIC INSUFFLATOR MODIFICATION

View all 38 devices →

Related Devices (Code: HHK)

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.

K251882Uterine Aspiration SetGcmedica Enterprise Ltd.(Wuxi)K240434RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)Li Medical Corporation , Ltd.K201952CrossGlide ETS PlusCrossbay MedicalK192534CrossBay Endometrial Tissue Sampler (ETS)Crossbay MedicalK102847DISPOSABLE ENDOMETRIAL SUCTION CURETTEJiangsu Suyun Medical Materials Co., Ltd.K092982THE PANPAC SUCTION CURETTEPanpac Medical Corporation

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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