MAVIG ANGIO SHIELD MODELS 6290 & 6272
K-Number: K934206 · 1993-10-07
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Device Summary
Frequently Asked Questions
What is the MAVIG ANGIO SHIELD MODELS 6290 & 6272?
MAVIG ANGIO SHIELD MODELS 6290 & 6272 is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is F. Walter Hanel GmbH. The 510(k) number is K934206.
When did MAVIG ANGIO SHIELD MODELS 6290 & 6272 receive FDA 510(k) clearance?
MAVIG ANGIO SHIELD MODELS 6290 & 6272 received FDA 510(k) clearance on 1993-10-07, under 510(k) number K934206.
Who is the listed applicant for MAVIG ANGIO SHIELD MODELS 6290 & 6272?
The FDA 510(k) record lists F. Walter Hanel GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAVIG ANGIO SHIELD MODELS 6290 & 6272?
The FDA product code for MAVIG ANGIO SHIELD MODELS 6290 & 6272 is KPY.
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 F. Walter Hanel 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.
Related Devices (Code: KPY)
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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