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)

DIAL-A-RAD PORTA RAD TABLE

K-Number: K913425 · 1992-11-24

ApplicantDial-A-Rad
Decision Date1992-11-24
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAL-A-RAD PORTA RAD TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Dial-A-Rad. It received FDA 510(k) clearance on 1992-11-24 under 510(k) number K913425. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAL-A-RAD PORTA RAD TABLE?

DIAL-A-RAD PORTA RAD TABLE is a medical device that received FDA 510(k) clearance on 1992-11-24. The listed applicant is Dial-A-Rad. The 510(k) number is K913425.

When did DIAL-A-RAD PORTA RAD TABLE receive FDA 510(k) clearance?

DIAL-A-RAD PORTA RAD TABLE received FDA 510(k) clearance on 1992-11-24, under 510(k) number K913425.

Who is the listed applicant for DIAL-A-RAD PORTA RAD TABLE?

The FDA 510(k) record lists Dial-A-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAL-A-RAD PORTA RAD TABLE?

The FDA product code for DIAL-A-RAD PORTA RAD TABLE is IXQ.

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.

Related Devices (Code: IXQ)

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.

↑