Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ACKRAD N-DO VAGE TUBE

K-Number: K813607 · 1982-02-05

Decision Date1982-02-05
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACKRAD N-DO VAGE TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Ackrad Laboratories. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K813607. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 42 devices →

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.

↑