A-DEC 2182 DOCTOR'S UNIT
K-Number: K925319 · 1993-12-09
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Device Summary
Frequently Asked Questions
What is the A-DEC 2182 DOCTOR'S UNIT?
A-DEC 2182 DOCTOR'S UNIT is a medical device that received FDA 510(k) clearance on 1993-12-09. The listed applicant is A-Dec, Inc.. The 510(k) number is K925319.
When did A-DEC 2182 DOCTOR'S UNIT receive FDA 510(k) clearance?
A-DEC 2182 DOCTOR'S UNIT received FDA 510(k) clearance on 1993-12-09, under 510(k) number K925319.
Who is the listed applicant for A-DEC 2182 DOCTOR'S UNIT?
The FDA 510(k) record lists A-Dec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A-DEC 2182 DOCTOR'S UNIT?
The FDA product code for A-DEC 2182 DOCTOR'S UNIT is KLC.
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 A-Dec, 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: KLC)
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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