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FDA 510(k)

GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS

K-Number: K081640 · 2009-05-06

ApplicantGimmi GmbH
Decision Date2009-05-06
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Gimmi GmbH. It received FDA 510(k) clearance on 2009-05-06 under 510(k) number K081640. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS?

GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS is a medical device that received FDA 510(k) clearance on 2009-05-06. The listed applicant is Gimmi GmbH. The 510(k) number is K081640.

When did GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS receive FDA 510(k) clearance?

GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS received FDA 510(k) clearance on 2009-05-06, under 510(k) number K081640.

Who is the listed applicant for GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS?

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

What is the FDA product code for GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS?

The FDA product code for GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS is HCH.

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Other records listing Gimmi GmbH 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.

K261179AlphaTriPart - Monopolar MIC InstrumentsK092421ALPHAHYSTEROSCOPE, FIBEROPTIC, OPERATIVE AND DIAGNOSTICK093125ALPHAXENON LIGHT 180 W AND 300 WK012869GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX, ZXXX.XX,S.XXXX.XX, K0142.25K012660GIMMI'ALPHA' ENDOSCOPES & ACCESSORIESK013731GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # E.8189.00/01/02/03

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Related Devices (Code: HCH)

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.

K211183Sugita AVM MicroclipsMizuho America, Inc.K180757D-Clip; D-Clip ApplierPeter Lazic GmbHK091921CODMAN ANEURYSM CLIPS, CODMAN AVM MICRO CLIP SYSTEM, CODMAN SLIM-LINE GRAFT, REINFORCING, MINI ANEURYSM CLIPCodman & Shurtleff, Inc.K081489L-ANEURYSM-CLIP SYSTEM & L-ANEURYSM CLIP APPLIERS, YASARGIL ANEURYSM CLIPS & YASARGIL ANEURYSM CLIP APPLIERSPeter Lazic GmbHK060915KIRWAN L-ANEURYSM CLIPS AND APPLIER, KIRWAN YASARGIL-TYPE ANEURYSM CLIPS AND APPLIERSKirwan Surgical Products, Inc.K043041AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX)Aesculap, 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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