ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU
K-Number: K962543 · 1996-09-11
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Device Summary
Frequently Asked Questions
What is the ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU?
ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU is a medical device that received FDA 510(k) clearance on 1996-09-11. The listed applicant is Nsk Nakanishi, Inc.. The 510(k) number is K962543.
When did ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU receive FDA 510(k) clearance?
ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU received FDA 510(k) clearance on 1996-09-11, under 510(k) number K962543.
Who is the listed applicant for ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU?
The FDA 510(k) record lists Nsk Nakanishi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU?
The FDA product code for ALPHA AIR HANDPIECE, ULTRA-PUSH, AL-SU, AL-MU, AL-TU 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 Nsk Nakanishi, 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: 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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