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FDA 510(k)

AUTOCHUCK ATTACHMENT

K-Number: K874294 · 1987-12-29

Decision Date1987-12-29
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AUTOCHUCK ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874294. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOCHUCK ATTACHMENT?

AUTOCHUCK ATTACHMENT is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. The 510(k) number is K874294.

When did AUTOCHUCK ATTACHMENT receive FDA 510(k) clearance?

AUTOCHUCK ATTACHMENT received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874294.

Who is the listed applicant for AUTOCHUCK ATTACHMENT?

The FDA 510(k) record lists Den-Tal-Ez Mfg Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOCHUCK ATTACHMENT?

The FDA product code for AUTOCHUCK ATTACHMENT is EFB.

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 Den-Tal-Ez Mfg Co., 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.

View all 7 devices →

Related Devices (Code: EFB)

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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