VINYL POLYSILOXANE IMPRESSION MATERIAL
K-Number: K800485 · 1980-03-18
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Device Summary
Frequently Asked Questions
What is the VINYL POLYSILOXANE IMPRESSION MATERIAL?
VINYL POLYSILOXANE IMPRESSION MATERIAL is a medical device that received FDA 510(k) clearance on 1980-03-18. The listed applicant is 3M Company. The 510(k) number is K800485.
When did VINYL POLYSILOXANE IMPRESSION MATERIAL receive FDA 510(k) clearance?
VINYL POLYSILOXANE IMPRESSION MATERIAL received FDA 510(k) clearance on 1980-03-18, under 510(k) number K800485.
Who is the listed applicant for VINYL POLYSILOXANE IMPRESSION MATERIAL?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL POLYSILOXANE IMPRESSION MATERIAL?
The FDA product code for VINYL POLYSILOXANE IMPRESSION MATERIAL 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 3M Company 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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