FDA 510(k)

MOGAN CIRCUMCISION CLAMP

K-Number: K926471 · 1994-02-25

Decision Date1994-02-25

Product CodeHFX

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

MOGAN CIRCUMCISION CLAMP 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 K926471. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOGAN CIRCUMCISION CLAMP?

MOGAN CIRCUMCISION CLAMP 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 K926471.

When did MOGAN CIRCUMCISION CLAMP receive FDA 510(k) clearance?

MOGAN CIRCUMCISION CLAMP received FDA 510(k) clearance on 1994-02-25, under 510(k) number K926471.

Who is the listed applicant for MOGAN CIRCUMCISION CLAMP?

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 MOGAN CIRCUMCISION CLAMP?

The FDA product code for MOGAN CIRCUMCISION CLAMP is HFX.

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Other records listing Thomasville Medical Assoc. as applicant

K926429VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT K926535GOMCO CIRCUMCISION CLAMP K926527ROTO FIT BIOPSY FORCEPS K926531HYSTERECTOMY FORCEPS K926532ENDO CERVICAL CURETTE K930030SUCTION TUBES: HOUSE, BARON

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Related Devices (Code: HFX)

K251687Konig Bell Circumcision ClampMedline Industries, LP K221356Wee BellWee Medical K212911Konig Mogen ClampMedline Industries, Inc.K131373SHANGRINGWuhu Snnda Medical Treatment Appliance Technology K121789SHANGRINGWuhu Snna Medical Treatment Appliance Technology C K103695PREPEX SYSTEMCirc Medtech

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.