VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES
K-Number: K022318 · 2002-09-19
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Device Summary
Frequently Asked Questions
What is the VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES?
VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES is a medical device that received FDA 510(k) clearance on 2002-09-19. The listed applicant is Vomed Volzer Medizintechnik GmbH & Co.. The 510(k) number is K022318.
When did VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES receive FDA 510(k) clearance?
VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES received FDA 510(k) clearance on 2002-09-19, under 510(k) number K022318.
Who is the listed applicant for VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES?
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 ENDOSCOPIC AND UROLOGICAL ACCESSORIES?
The FDA product code for VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES is HIF.
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.
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.
Related Devices (Code: HIF)
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.
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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