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FDA 510(k)

REUSABLE JACOBS DRILL CHUCK

K-Number: K853495 · 1985-09-05

ApplicantChattanooga Group, Inc.
Decision Date1985-09-05
Product Code
DecisionSubstantially Equivalent

Device Summary

REUSABLE JACOBS DRILL CHUCK is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K853495. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE JACOBS DRILL CHUCK?

REUSABLE JACOBS DRILL CHUCK is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K853495.

When did REUSABLE JACOBS DRILL CHUCK receive FDA 510(k) clearance?

REUSABLE JACOBS DRILL CHUCK received FDA 510(k) clearance on 1985-09-05, under 510(k) number K853495.

Who is the listed applicant for REUSABLE JACOBS DRILL CHUCK?

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

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Other records listing Chattanooga Group, 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.

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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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