VAN-TEC ENDOPYELOTOMY KNIFE
K-Number: K880094 · 1988-02-29
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Device Summary
Frequently Asked Questions
What is the VAN-TEC ENDOPYELOTOMY KNIFE?
VAN-TEC ENDOPYELOTOMY KNIFE is a medical device that received FDA 510(k) clearance on 1988-02-29. The listed applicant is Van-Tec, Inc.. The 510(k) number is K880094.
When did VAN-TEC ENDOPYELOTOMY KNIFE receive FDA 510(k) clearance?
VAN-TEC ENDOPYELOTOMY KNIFE received FDA 510(k) clearance on 1988-02-29, under 510(k) number K880094.
Who is the listed applicant for VAN-TEC ENDOPYELOTOMY KNIFE?
The FDA 510(k) record lists Van-Tec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VAN-TEC ENDOPYELOTOMY KNIFE?
The FDA product code for VAN-TEC ENDOPYELOTOMY KNIFE is EMF.
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 Van-Tec, 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: EMF)
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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