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FDA 510(k)

KEVOR-CURETTE

K-Number: K882404 · 1988-07-08

ApplicantEuro-Med Intl.
Decision Date1988-07-08
Product CodePCF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KEVOR-CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Euro-Med Intl.. It received FDA 510(k) clearance on 1988-07-08 under 510(k) number K882404. The device is classified under product code PCF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEVOR-CURETTE?

KEVOR-CURETTE is a medical device that received FDA 510(k) clearance on 1988-07-08. The listed applicant is Euro-Med Intl.. The 510(k) number is K882404.

When did KEVOR-CURETTE receive FDA 510(k) clearance?

KEVOR-CURETTE received FDA 510(k) clearance on 1988-07-08, under 510(k) number K882404.

Who is the listed applicant for KEVOR-CURETTE?

The FDA 510(k) record lists Euro-Med Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KEVOR-CURETTE?

The FDA product code for KEVOR-CURETTE is PCF.

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 Euro-Med Intl. 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.

K883884PROSTATIC CORE-CUT NEEDLEK854894SPOONK854901PACIFIC GRASPERK854891KNIFEK854890HOOK PROBEK854895BASKET FORCEP

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Related Devices (Code: PCF)

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.

K122658FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009Femasys, Inc.K060320FEMECC ENDOCERVICAL CURETTEFemspec LLCK882606EURO-MED ENDO-CURETTEBuckman Co., Inc.K860796DISPO-URETTERoland J. Zwick, 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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