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FDA 510(k)

LSVP INTERNATIONAL BIOPSY FORCEPS

K-Number: K944770 · 1994-10-13

ApplicantLsvp Intl., Inc.
Decision Date1994-10-13
Product CodeFCL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LSVP INTERNATIONAL BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Lsvp Intl., Inc.. It received FDA 510(k) clearance on 1994-10-13 under 510(k) number K944770. 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 LSVP INTERNATIONAL BIOPSY FORCEPS?

LSVP INTERNATIONAL BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1994-10-13. The listed applicant is Lsvp Intl., Inc.. The 510(k) number is K944770.

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

LSVP INTERNATIONAL BIOPSY FORCEPS received FDA 510(k) clearance on 1994-10-13, under 510(k) number K944770.

Who is the listed applicant for LSVP INTERNATIONAL BIOPSY FORCEPS?

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

What is the FDA product code for LSVP INTERNATIONAL BIOPSY FORCEPS?

The FDA product code for LSVP INTERNATIONAL BIOPSY FORCEPS is FCL.

Related Clinical Trials

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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Other records listing Lsvp Intl., 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.

K982983LSVP INTERNATIONAL BIOPSY FORCEPSK971204LSVP INTERNATIONAL HOT BIOPSY FORCEPSK945295LSVP INTERNATIONAL GRASPING FORCEPS

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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