ACKRAD N-DO VAGE TUBE
K-Number: K813607 · 1982-02-05
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Device Summary
Frequently Asked Questions
What is the ACKRAD N-DO VAGE TUBE?
ACKRAD N-DO VAGE TUBE is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Ackrad Laboratories. The 510(k) number is K813607.
When did ACKRAD N-DO VAGE TUBE receive FDA 510(k) clearance?
ACKRAD N-DO VAGE TUBE received FDA 510(k) clearance on 1982-02-05, under 510(k) number K813607.
Who is the listed applicant for ACKRAD N-DO VAGE TUBE?
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 N-DO VAGE TUBE?
The FDA product code for ACKRAD N-DO VAGE TUBE is FQH.
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: FQH)
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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