FDA 510(k)

ATRAUMATIC TENACULA

K-Number: K930037 · 1994-02-24

Decision Date1994-02-24

Product CodeHDC

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

ATRAUMATIC TENACULA 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 1994-02-24 under 510(k) number K930037. The device is classified under product code HDC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATRAUMATIC TENACULA?

ATRAUMATIC TENACULA is a medical device that received FDA 510(k) clearance on 1994-02-24. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K930037.

When did ATRAUMATIC TENACULA receive FDA 510(k) clearance?

ATRAUMATIC TENACULA received FDA 510(k) clearance on 1994-02-24, under 510(k) number K930037.

Who is the listed applicant for ATRAUMATIC TENACULA?

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 ATRAUMATIC TENACULA?

The FDA product code for ATRAUMATIC TENACULA is HDC.

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Other records listing Thomasville Medical Assoc. as applicant

K926429VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT K926471MOGAN CIRCUMCISION CLAMP K926527ROTO FIT BIOPSY FORCEPS K926535GOMCO CIRCUMCISION CLAMP K926532ENDO CERVICAL CURETTE K926531HYSTERECTOMY FORCEPS

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Related Devices (Code: HDC)

K223866Carevix™ Suction Cervical StabilizerAspivix SA K203820ASPIVIX v1.1 Cervical Suction TenaculumAspivix SA K082349JARIT HULKA UTERINE TENACULUM FORCEPSJ. Jamner Surgical Instruments, Inc.K073182GYN DISPOSABLES TENACULUM 356TGyn-Disposables, Inc.K062563FEMTEN CERVICAL TENACULUMFem Suite, LLC K060573BURBANK TENACULUMVascular Control Systems, 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.