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FDA 510(k)

CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON

K-Number: K930034 · 1994-02-24

ApplicantThomasville Medical Assoc.
Decision Date1994-02-24
Product CodeHDQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON 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 K930034. The device is classified under product code HDQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON?

CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON 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 K930034.

When did CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON receive FDA 510(k) clearance?

CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON received FDA 510(k) clearance on 1994-02-24, under 510(k) number K930034.

Who is the listed applicant for CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON?

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 CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON?

The FDA product code for CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTON is HDQ.

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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, INFANTK926471MOGAN CIRCUMCISION CLAMPK926527ROTO FIT BIOPSY FORCEPSK926535GOMCO CIRCUMCISION CLAMPK926532ENDO CERVICAL CURETTEK926531HYSTERECTOMY FORCEPS

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Related Devices (Code: HDQ)

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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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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