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FDA 510(k)

VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT

K-Number: K926429 · 1994-02-28

ApplicantThomasville Medical Assoc.
Decision Date1994-02-28
Product CodeHDF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT 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 1994-02-28 under 510(k) number K926429. The device is classified under product code HDF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT?

VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K926429.

When did VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT receive FDA 510(k) clearance?

VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT received FDA 510(k) clearance on 1994-02-28, under 510(k) number K926429.

Who is the listed applicant for VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT?

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 VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT?

The FDA product code for VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT is HDF.

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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.

K926531HYSTERECTOMY FORCEPSK926535GOMCO CIRCUMCISION CLAMPK926471MOGAN CIRCUMCISION CLAMPK926532ENDO CERVICAL CURETTEK926527ROTO FIT BIOPSY FORCEPSK930030SUCTION TUBES: HOUSE, BARON

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Related Devices (Code: HDF)

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.

K902019MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPSGynescope Corp.K891041MIYA SPECULUMZinnanti Surgical Instruments, Inc.K891044LASER SPECULAZinnanti Surgical Instruments, Inc.K890375VAGINAL SPECULUMKinetic Medical ProductsK862478HAYES VAGINAL SHIELDFranklin Medical USA, Inc.K853640WELLINGTON HOSPITAL PATTERN SELF RETAINING VAGINALDowns Surgical , Ltd.

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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