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FDA 510(k)

CANNULATED BIOPSY FORCEPS

K-Number: K926430 · 1993-03-26

ApplicantThomasville Medical Assoc.
Decision Date1993-03-26
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CANNULATED BIOPSY FORCEPS 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 1993-03-26 under 510(k) number K926430. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULATED BIOPSY FORCEPS?

CANNULATED BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1993-03-26. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K926430.

When did CANNULATED BIOPSY FORCEPS receive FDA 510(k) clearance?

CANNULATED BIOPSY FORCEPS received FDA 510(k) clearance on 1993-03-26, under 510(k) number K926430.

Who is the listed applicant for CANNULATED BIOPSY FORCEPS?

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 CANNULATED BIOPSY FORCEPS?

The FDA product code for CANNULATED BIOPSY FORCEPS is EOQ.

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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 CLAMPK926535GOMCO CIRCUMCISION CLAMPK926532ENDO CERVICAL CURETTEK926527ROTO FIT BIOPSY FORCEPSK926531HYSTERECTOMY FORCEPS

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Related Devices (Code: EOQ)

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.

K261637Single-use Flexible BronchoscopeHunan Vathin Medical Instrument Co., Ltd.K260309Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler SetAmbu A/SK2540263.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U)Flexicare Medical Limited.K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.K254037LungFlow Airway CatheterFree Flow Medical, Inc.K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TFujifilm Corporation

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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