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FDA 510(k)

LSVP INTERNATIONAL BIOPSY FORCEPS

K-Number: K982983 · 1998-09-29

ApplicantLsvp Intl., Inc.
Decision Date1998-09-29
Product CodeEOQ
Advisory CommitteeEN
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 1998-09-29 under 510(k) number K982983. 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 LSVP INTERNATIONAL BIOPSY FORCEPS?

LSVP INTERNATIONAL BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1998-09-29. The listed applicant is Lsvp Intl., Inc.. The 510(k) number is K982983.

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

LSVP INTERNATIONAL BIOPSY FORCEPS received FDA 510(k) clearance on 1998-09-29, under 510(k) number K982983.

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 EOQ.

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.

K971204LSVP INTERNATIONAL HOT BIOPSY FORCEPSK945295LSVP INTERNATIONAL GRASPING FORCEPSK944770LSVP INTERNATIONAL BIOPSY FORCEPS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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