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FDA 510(k)

GIP/MEDI-GLOBE BIOPSY FORCEPS

K-Number: K941359 · 1994-07-12

ApplicantMedi-Globe Corp.
Decision Date1994-07-12
Product CodeFCL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GIP/MEDI-GLOBE BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Globe Corp.. It received FDA 510(k) clearance on 1994-07-12 under 510(k) number K941359. The device is classified under product code FCL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIP/MEDI-GLOBE BIOPSY FORCEPS?

GIP/MEDI-GLOBE BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1994-07-12. The listed applicant is Medi-Globe Corp.. The 510(k) number is K941359.

When did GIP/MEDI-GLOBE BIOPSY FORCEPS receive FDA 510(k) clearance?

GIP/MEDI-GLOBE BIOPSY FORCEPS received FDA 510(k) clearance on 1994-07-12, under 510(k) number K941359.

Who is the listed applicant for GIP/MEDI-GLOBE BIOPSY FORCEPS?

The FDA 510(k) record lists Medi-Globe Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GIP/MEDI-GLOBE BIOPSY FORCEPS?

The FDA product code for GIP/MEDI-GLOBE BIOPSY FORCEPS is FCL.

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Other records listing Medi-Globe Corp. 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.

K061222INJECTRA INJECTION NEEDLEK051247SONOTIP II ULTRASOUND NEEDLE SYSTEMK011261STONE EXTRACTOR BALLOON CATHETERK010714EXPANDER, MODELS 1400880, 1401280, 1401680, 1401880, 1410420, 1410620, 1410830K010549BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)K990220MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM

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Related Devices (Code: FCL)

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.

K032092OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPEOlympus Optical Co., Ltd.K973611SPECTRASCIENCE REUSABLE BIOPSY FORCEPSSpectrascience, Inc.K971315AUXILIARY INSTRUMENTS FOR URSRichard Wolf Medical Instruments Corp.K964120INJECTO FLUSHRobert J. Jynch, Jr.K963517SPECTRA SCIENCE BIOPSY FORCEPSSpectrascience, Inc.K955065OLYMPUS FB SERIES BIOPSY FORCEPSOlympus America, 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.

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