IMPRESSION MATERIAL, RUBBER
K-Number: K790592 · 1979-06-15
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Device Summary
Frequently Asked Questions
What is the IMPRESSION MATERIAL, RUBBER?
IMPRESSION MATERIAL, RUBBER is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Wallace A. Erickson & Co.. The 510(k) number is K790592.
When did IMPRESSION MATERIAL, RUBBER receive FDA 510(k) clearance?
IMPRESSION MATERIAL, RUBBER received FDA 510(k) clearance on 1979-06-15, under 510(k) number K790592.
Who is the listed applicant for IMPRESSION MATERIAL, RUBBER?
The FDA 510(k) record lists Wallace A. Erickson & Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMPRESSION MATERIAL, RUBBER?
The FDA product code for IMPRESSION MATERIAL, RUBBER 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 Wallace A. Erickson & Co. 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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