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FDA 510(k)

ODONTIC CENTRIC(BITE) REGIST. PASTE

K-Number: K830044 · 1983-04-06

Decision Date1983-04-06
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ODONTIC CENTRIC(BITE) REGIST. PASTE 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 1983-04-06 under 510(k) number K830044. 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 ODONTIC CENTRIC(BITE) REGIST. PASTE?

ODONTIC CENTRIC(BITE) REGIST. PASTE is a medical device that received FDA 510(k) clearance on 1983-04-06. The listed applicant is Wallace A. Erickson & Co.. The 510(k) number is K830044.

When did ODONTIC CENTRIC(BITE) REGIST. PASTE receive FDA 510(k) clearance?

ODONTIC CENTRIC(BITE) REGIST. PASTE received FDA 510(k) clearance on 1983-04-06, under 510(k) number K830044.

Who is the listed applicant for ODONTIC CENTRIC(BITE) REGIST. PASTE?

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 ODONTIC CENTRIC(BITE) REGIST. PASTE?

The FDA product code for ODONTIC CENTRIC(BITE) REGIST. PASTE 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.

View all 32 devices →

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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