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FDA 510(k)

DENTA A-33

K-Number: K830439 · 1983-05-09

ApplicantDenta, Inc.
Decision Date1983-05-09
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTA A-33 is the device name listed in this FDA 510(k) record. The listed applicant is Denta, Inc.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K830439. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTA A-33?

DENTA A-33 is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Denta, Inc.. The 510(k) number is K830439.

When did DENTA A-33 receive FDA 510(k) clearance?

DENTA A-33 received FDA 510(k) clearance on 1983-05-09, under 510(k) number K830439.

Who is the listed applicant for DENTA A-33?

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

What is the FDA product code for DENTA A-33?

The FDA product code for DENTA A-33 is EGG.

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.

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Other records listing Denta, Inc. 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.

K830440DENTA PLAST

Related Devices (Code: EGG)

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.

K990979STECO-TITANMAGNETICSSteco-System-Technik GmbH & CokgK950259COUPLING DEVICE FOR DENTAL PROSTHESISDr. Joseph E. Grasso, D.D.S.K925700ZEST ANCHOR ADVANCED GENERATIONZest Anchors, Inc.K915299COGAN CORP KITS OF DENTAL HAND INSTRUMENTSCogan Corp.K912435DENTAL CONNECTOR PRECISION ATTACHMENTMetalor Dental USA Corp.K912567CONICAST, INTRACAST, OMECASTMetalor Dental USA Corp.

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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