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FDA 510(k)

CURETTE, PROPOSED TIS-U-TRAP, METAL

K-Number: K760264 · 1976-10-06

ApplicantMilex Products, Inc.
Decision Date1976-10-06
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CURETTE, PROPOSED TIS-U-TRAP, METAL is the device name listed in this FDA 510(k) record. The listed applicant is Milex Products, Inc.. It received FDA 510(k) clearance on 1976-10-06 under 510(k) number K760264. 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 CURETTE, PROPOSED TIS-U-TRAP, METAL?

CURETTE, PROPOSED TIS-U-TRAP, METAL is a medical device that received FDA 510(k) clearance on 1976-10-06. The listed applicant is Milex Products, Inc.. The 510(k) number is K760264.

When did CURETTE, PROPOSED TIS-U-TRAP, METAL receive FDA 510(k) clearance?

CURETTE, PROPOSED TIS-U-TRAP, METAL received FDA 510(k) clearance on 1976-10-06, under 510(k) number K760264.

Who is the listed applicant for CURETTE, PROPOSED TIS-U-TRAP, METAL?

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

What is the FDA product code for CURETTE, PROPOSED TIS-U-TRAP, METAL?

The FDA product code for CURETTE, PROPOSED TIS-U-TRAP, METAL is HHK.

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Other records listing Milex 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.

K001545PIPET CURETK904774INGLAT-O-BALLK904026INFLAT-O-BALLK900903KOPANS HOOKWIRE LESION LOCALIZATION NEEDLEK882628ENDO C BRUSHK862410MILEX KEGEL PERINEAL EXERCISER

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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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