VOYAGE
K-Number: K930949 · 1993-06-01
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Device Summary
Frequently Asked Questions
What is the VOYAGE?
VOYAGE is a medical device that received FDA 510(k) clearance on 1993-06-01. The listed applicant is Mada Medical Products, Inc.. The 510(k) number is K930949.
When did VOYAGE receive FDA 510(k) clearance?
VOYAGE received FDA 510(k) clearance on 1993-06-01, under 510(k) number K930949.
Who is the listed applicant for VOYAGE?
The FDA 510(k) record lists Mada Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOYAGE?
The FDA product code for VOYAGE is CAF.
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 Mada Medical Products, Inc. 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: CAF)
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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