PEMACO 3000 INTRAORAL DENTAL WAX
K-Number: K895561 · 1989-11-06
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Device Summary
Frequently Asked Questions
What is the PEMACO 3000 INTRAORAL DENTAL WAX?
PEMACO 3000 INTRAORAL DENTAL WAX is a medical device that received FDA 510(k) clearance on 1989-11-06. The listed applicant is Pemaco, Inc.. The 510(k) number is K895561.
When did PEMACO 3000 INTRAORAL DENTAL WAX receive FDA 510(k) clearance?
PEMACO 3000 INTRAORAL DENTAL WAX received FDA 510(k) clearance on 1989-11-06, under 510(k) number K895561.
Who is the listed applicant for PEMACO 3000 INTRAORAL DENTAL WAX?
The FDA 510(k) record lists Pemaco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PEMACO 3000 INTRAORAL DENTAL WAX?
The FDA product code for PEMACO 3000 INTRAORAL DENTAL WAX is EGD.
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 Pemaco, 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: EGD)
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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