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FDA 510(k)

GLOBAL MEDICAL CUTTING BIOPSY NEEDLE

K-Number: K934256 · 1994-03-28

ApplicantGlobal Medical Prods, Inc.
Decision Date1994-03-28
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GLOBAL MEDICAL CUTTING BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Global Medical Prods, Inc.. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K934256. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOBAL MEDICAL CUTTING BIOPSY NEEDLE?

GLOBAL MEDICAL CUTTING BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Global Medical Prods, Inc.. The 510(k) number is K934256.

When did GLOBAL MEDICAL CUTTING BIOPSY NEEDLE receive FDA 510(k) clearance?

GLOBAL MEDICAL CUTTING BIOPSY NEEDLE received FDA 510(k) clearance on 1994-03-28, under 510(k) number K934256.

Who is the listed applicant for GLOBAL MEDICAL CUTTING BIOPSY NEEDLE?

The FDA 510(k) record lists Global Medical Prods, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLOBAL MEDICAL CUTTING BIOPSY NEEDLE?

The FDA product code for GLOBAL MEDICAL CUTTING BIOPSY NEEDLE is FCG.

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Other records listing Global Medical Prods, Inc. 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.

K962329GLOBAL LOSS OF RESISTANCE SYRINGE GLOR 10K961324GLOBAL MEDICAL PRODUCTS SPINAL,CONICAL TIP (SPROTTLE STYLE), WHITACRE STYLE NEEDLESK952275GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUBK871556MERIVAARA EMERGENCY PATIENT TROLLEY #436K863748HOSPITAL BEDK862959MERIVAARA PATIENT TROLLEY - MODEL #416

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Related Devices (Code: FCG)

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.

K252646Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)Olympus Medical Systems Corp.K250994ClearTip FNA and FNB TypesFinemedix Co., Ltd.K241209EchoTip AcuCore™ EUS Biopsy Needle (ECHO-BX-19)Cook Ireland, Ltd.K231422Precision GILimaca Medical, Ltd.K231267ClearTipFinemedix Co., Ltd.K230909EchoTip® AcuCore™ Ultrasound Biopsy Needle (ECHO-BX-3-22)Cook Ireland, 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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