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FDA 510(k)

ENDO CERVICAL CURETTE

K-Number: K926532 · 1994-02-25

ApplicantThomasville Medical Assoc.
Decision Date1994-02-25
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDO CERVICAL CURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Thomasville Medical Assoc.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K926532. The device is classified under product code KNA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO CERVICAL CURETTE?

ENDO CERVICAL CURETTE is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K926532.

When did ENDO CERVICAL CURETTE receive FDA 510(k) clearance?

ENDO CERVICAL CURETTE received FDA 510(k) clearance on 1994-02-25, under 510(k) number K926532.

Who is the listed applicant for ENDO CERVICAL CURETTE?

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

What is the FDA product code for ENDO CERVICAL CURETTE?

The FDA product code for ENDO CERVICAL CURETTE is KNA.

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Other records listing Thomasville Medical Assoc. 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.

K926429VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTK926535GOMCO CIRCUMCISION CLAMPK926471MOGAN CIRCUMCISION CLAMPK926527ROTO FIT BIOPSY FORCEPSK926531HYSTERECTOMY FORCEPSK930030SUCTION TUBES: HOUSE, BARON

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Related Devices (Code: KNA)

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.

K102141COOK WORD BARTHOLIN GLAND CATHETER (FINAL TRADE NAME NOT YET DETERMINED)Cook Urological, Inc.K093904GLENVEIGH VAGINAL TAMPONADE BALLOON CATHETERGlenveigh Surgical, LLCK082939COOK FETAL MEMBRANE MANIPULATOR, MODEL -FMM-122400Cook Urological, Inc.K062438BAKRI POSTPARTUM BALLOON, MODEL J-SOS-100500Cook Ob/GynK060289EPISTAT, V-STAT, MODELS EPISTAT-001-01, V-STAT-001-01Frontline MedicalK013597TAMPONADE UTERINE BALLOON CATHETER SETCook Ob/Gyn

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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