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FDA 510(k)

OLYPUS FG SERIES GRASPING FORCEPS

K-Number: K962533 · 1996-08-09

ApplicantOlympus America, Inc.
Decision Date1996-08-09
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

OLYPUS FG SERIES GRASPING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America, Inc.. It received FDA 510(k) clearance on 1996-08-09 under 510(k) number K962533. 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 OLYPUS FG SERIES GRASPING FORCEPS?

OLYPUS FG SERIES GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1996-08-09. The listed applicant is Olympus America, Inc.. The 510(k) number is K962533.

When did OLYPUS FG SERIES GRASPING FORCEPS receive FDA 510(k) clearance?

OLYPUS FG SERIES GRASPING FORCEPS received FDA 510(k) clearance on 1996-08-09, under 510(k) number K962533.

Who is the listed applicant for OLYPUS FG SERIES GRASPING FORCEPS?

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

What is the FDA product code for OLYPUS FG SERIES GRASPING FORCEPS?

The FDA product code for OLYPUS FG SERIES GRASPING FORCEPS is EOQ.

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Other records listing Olympus America, 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.

K111788ENDOEYE HD IIK081615OLYMPUS CEA - CARCINOEMBRYONIC ANTIGENK073487OLYMPUS IGM REAGENTK073490OLYMPUS IGG REAGENTK073489OLYMPUS IGA REAGENTK062862OLYMPUS URIC ACID REAGENT, MODEL OSR6X98

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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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