CLARK PRECISION BLOCK CUTTER, COOLING
K-Number: K842615 · 1984-09-04
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Device Summary
Frequently Asked Questions
What is the CLARK PRECISION BLOCK CUTTER, COOLING?
CLARK PRECISION BLOCK CUTTER, COOLING is a medical device that received FDA 510(k) clearance on 1984-09-04. The listed applicant is Clark Research and Development, Inc.. The 510(k) number is K842615.
When did CLARK PRECISION BLOCK CUTTER, COOLING receive FDA 510(k) clearance?
CLARK PRECISION BLOCK CUTTER, COOLING received FDA 510(k) clearance on 1984-09-04, under 510(k) number K842615.
Who is the listed applicant for CLARK PRECISION BLOCK CUTTER, COOLING?
The FDA 510(k) record lists Clark Research and Development, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLARK PRECISION BLOCK CUTTER, COOLING?
The FDA product code for CLARK PRECISION BLOCK CUTTER, COOLING is IXI.
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 Clark Research and Development, 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.
Related Devices (Code: IXI)
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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