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FDA 510(k)

TEMP. CROWN ACRYLIC RESIN

K-Number: K771530 · 1977-08-25

Decision Date1977-08-25
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEMP. CROWN ACRYLIC RESIN is the device name listed in this FDA 510(k) record. The listed applicant is J. Palmero Sales Co., Inc.. It received FDA 510(k) clearance on 1977-08-25 under 510(k) number K771530. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP. CROWN ACRYLIC RESIN?

TEMP. CROWN ACRYLIC RESIN is a medical device that received FDA 510(k) clearance on 1977-08-25. The listed applicant is J. Palmero Sales Co., Inc.. The 510(k) number is K771530.

When did TEMP. CROWN ACRYLIC RESIN receive FDA 510(k) clearance?

TEMP. CROWN ACRYLIC RESIN received FDA 510(k) clearance on 1977-08-25, under 510(k) number K771530.

Who is the listed applicant for TEMP. CROWN ACRYLIC RESIN?

The FDA 510(k) record lists J. Palmero Sales Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMP. CROWN ACRYLIC RESIN?

The FDA product code for TEMP. CROWN ACRYLIC RESIN is EBG.

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.

Related Devices (Code: EBG)

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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