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FDA 510(k)

VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000

K-Number: K023019 · 2002-12-10

ApplicantVomed Volzer Medizintechnik GmbH & Co.
Decision Date2002-12-10
Product CodeFGI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 is the device name listed in this FDA 510(k) record. The listed applicant is Vomed Volzer Medizintechnik GmbH & Co.. It received FDA 510(k) clearance on 2002-12-10 under 510(k) number K023019. The device is classified under product code FGI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000?

VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 is a medical device that received FDA 510(k) clearance on 2002-12-10. The listed applicant is Vomed Volzer Medizintechnik GmbH & Co.. The 510(k) number is K023019.

When did VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 receive FDA 510(k) clearance?

VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 received FDA 510(k) clearance on 2002-12-10, under 510(k) number K023019.

Who is the listed applicant for VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000?

The FDA 510(k) record lists Vomed Volzer Medizintechnik GmbH & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000?

The FDA product code for VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 is FGI.

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Other records listing Vomed Volzer Medizintechnik GmbH & Co. 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.

K022257VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 XXX & 9006 XXX-9011 XXXK022318VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES

Related Devices (Code: FGI)

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.

K013360DFINER UROLOGICAL CATHETERNeoseed Technology,LlcK810370POLLACK CHAIN CYSOURETHROGRAM SETVance Products, Inc.

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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