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FDA 510(k)

AMSINO CERVICAL SCRAPER

K-Number: K950780 · 1995-07-25

ApplicantAmsino Intl., Inc.
Decision Date1995-07-25
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AMSINO CERVICAL SCRAPER is the device name listed in this FDA 510(k) record. The listed applicant is Amsino Intl., Inc.. It received FDA 510(k) clearance on 1995-07-25 under 510(k) number K950780. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSINO CERVICAL SCRAPER?

AMSINO CERVICAL SCRAPER is a medical device that received FDA 510(k) clearance on 1995-07-25. The listed applicant is Amsino Intl., Inc.. The 510(k) number is K950780.

When did AMSINO CERVICAL SCRAPER receive FDA 510(k) clearance?

AMSINO CERVICAL SCRAPER received FDA 510(k) clearance on 1995-07-25, under 510(k) number K950780.

Who is the listed applicant for AMSINO CERVICAL SCRAPER?

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

What is the FDA product code for AMSINO CERVICAL SCRAPER?

The FDA product code for AMSINO CERVICAL SCRAPER is HHT.

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Other records listing Amsino Intl., 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.

K070873AMSURE BLADDER IRRIGATION SETK992719AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKEK974042AMSURE CLEANSING ENEMA SETK973107AMSINO I.V. ADMINISTRATION SETK973199AMSINO SUCTION CATHETERK971929AMSINO URINARY LEG BAG

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Related Devices (Code: HHT)

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.

K182049exCellerator Cervical Collection DeviceExcell Company, LLCK153128Kolplast Cervical Sample Collection KitKolplast CI SAK111681HISTOBRUSHPuritan Medical Products Company, LLCK083012PAPCONEOtto Bock Pur Life Science GmbHK081522BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGYBio Nuclear Diagnostics, Inc.K072381SOFTPAP CERVICAL CELL COLLECTORCytocore, Inc.

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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