TRADITION P, PUSH BUTTON HANDPIECE
K-Number: K963050 · 1996-10-11
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Device Summary
Frequently Asked Questions
What is the TRADITION P, PUSH BUTTON HANDPIECE?
TRADITION P, PUSH BUTTON HANDPIECE is a medical device that received FDA 510(k) clearance on 1996-10-11. The listed applicant is Midwest Dental Products Corp.. The 510(k) number is K963050.
When did TRADITION P, PUSH BUTTON HANDPIECE receive FDA 510(k) clearance?
TRADITION P, PUSH BUTTON HANDPIECE received FDA 510(k) clearance on 1996-10-11, under 510(k) number K963050.
Who is the listed applicant for TRADITION P, PUSH BUTTON HANDPIECE?
The FDA 510(k) record lists Midwest Dental Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRADITION P, PUSH BUTTON HANDPIECE?
The FDA product code for TRADITION P, PUSH BUTTON HANDPIECE is EFB.
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 Midwest Dental Products Corp. 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: EFB)
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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