ABSOLUTE VINYL POLYSILOXANE IMPRESS
K-Number: K842877 · 1985-03-11
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Device Summary
Frequently Asked Questions
What is the ABSOLUTE VINYL POLYSILOXANE IMPRESS?
ABSOLUTE VINYL POLYSILOXANE IMPRESS is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Coe Laboratories, Inc.. The 510(k) number is K842877.
When did ABSOLUTE VINYL POLYSILOXANE IMPRESS receive FDA 510(k) clearance?
ABSOLUTE VINYL POLYSILOXANE IMPRESS received FDA 510(k) clearance on 1985-03-11, under 510(k) number K842877.
Who is the listed applicant for ABSOLUTE VINYL POLYSILOXANE IMPRESS?
The FDA 510(k) record lists Coe Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABSOLUTE VINYL POLYSILOXANE IMPRESS?
The FDA product code for ABSOLUTE VINYL POLYSILOXANE IMPRESS is ELW.
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 Coe Laboratories, 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: ELW)
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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