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FDA 510(k)

SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN

K-Number: K932266 · 1994-03-15

ApplicantSymbiosis Corp.
Decision Date1994-03-15
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1994-03-15 under 510(k) number K932266. The device is classified under product code KGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN?

SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN is a medical device that received FDA 510(k) clearance on 1994-03-15. The listed applicant is Symbiosis Corp.. The 510(k) number is K932266.

When did SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN receive FDA 510(k) clearance?

SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN received FDA 510(k) clearance on 1994-03-15, under 510(k) number K932266.

Who is the listed applicant for SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN?

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

What is the FDA product code for SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN?

The FDA product code for SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN is KGE.

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Other records listing Symbiosis 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.

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESK952432SYMBIOSIS BIPOLAR FORCEPSK951387SYMBIOSIS BIPOLAR SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORS

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Related Devices (Code: KGE)

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.

K251807Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LROlympus Medical Systems Corp.K250187Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)Olympus Medical Systems CorporationK242857ClearHemograsperFinemedix Co., Ltd.K231721Disposable Hot Biopsy ForcepsBeijing Zksk Technology Co., Ltd.K220053Diathermic Slitter (FlushKnife) DK2620JI and DK2623JIFujifilm CorporationK210406Bipolar Coagulation ForecepsHangzhou AGS MedTech Co., 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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