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FDA 510(k)

IMPRESSION MATERIAL, RUBBER

K-Number: K790592 · 1979-06-15

Decision Date1979-06-15
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPRESSION MATERIAL, RUBBER is the device name listed in this FDA 510(k) record. The listed applicant is Wallace A. Erickson & Co.. It received FDA 510(k) clearance on 1979-06-15 under 510(k) number K790592. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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