ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE)
K-Number: K895854 · 1990-04-09
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Device Summary
Frequently Asked Questions
What is the ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE)?
ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE) is a medical device that received FDA 510(k) clearance on 1990-04-09. The listed applicant is Acme-Monaco Corp.. The 510(k) number is K895854.
When did ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE) receive FDA 510(k) clearance?
ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE) received FDA 510(k) clearance on 1990-04-09, under 510(k) number K895854.
Who is the listed applicant for ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE)?
The FDA 510(k) record lists Acme-Monaco Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE)?
The FDA product code for ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE) is EJF.
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 Acme-Monaco 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: EJF)
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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