NIPPER, PSO4 TISSUE
K-Number: K770301 · 1977-03-07
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Device Summary
Frequently Asked Questions
What is the NIPPER, PSO4 TISSUE?
NIPPER, PSO4 TISSUE is a medical device that received FDA 510(k) clearance on 1977-03-07. The listed applicant is Dentronix, Inc.. The 510(k) number is K770301.
When did NIPPER, PSO4 TISSUE receive FDA 510(k) clearance?
NIPPER, PSO4 TISSUE received FDA 510(k) clearance on 1977-03-07, under 510(k) number K770301.
Who is the listed applicant for NIPPER, PSO4 TISSUE?
The FDA 510(k) record lists Dentronix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NIPPER, PSO4 TISSUE?
The FDA product code for NIPPER, PSO4 TISSUE is FZT.
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 Dentronix, 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: FZT)
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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