ACKRAD INCISION & DRAIN SET
K-Number: K813103 · 1981-12-09
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Device Summary
Frequently Asked Questions
What is the ACKRAD INCISION & DRAIN SET?
ACKRAD INCISION & DRAIN SET is a medical device that received FDA 510(k) clearance on 1981-12-09. The listed applicant is Ackrad Laboratories. The 510(k) number is K813103.
When did ACKRAD INCISION & DRAIN SET receive FDA 510(k) clearance?
ACKRAD INCISION & DRAIN SET received FDA 510(k) clearance on 1981-12-09, under 510(k) number K813103.
Who is the listed applicant for ACKRAD INCISION & DRAIN SET?
The FDA 510(k) record lists Ackrad Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACKRAD INCISION & DRAIN SET?
The FDA product code for ACKRAD INCISION & DRAIN SET is KDD.
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 Ackrad Laboratories 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: KDD)
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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