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)

VRT TABLE W/INTEGRATING TUBE STAND/ELEV

K-Number: K813173 · 1981-12-14

Decision Date1981-12-14
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VRT TABLE W/INTEGRATING TUBE STAND/ELEV is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1981-12-14 under 510(k) number K813173. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VRT TABLE W/INTEGRATING TUBE STAND/ELEV?

VRT TABLE W/INTEGRATING TUBE STAND/ELEV is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is General Electric Co.. The 510(k) number is K813173.

When did VRT TABLE W/INTEGRATING TUBE STAND/ELEV receive FDA 510(k) clearance?

VRT TABLE W/INTEGRATING TUBE STAND/ELEV received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813173.

Who is the listed applicant for VRT TABLE W/INTEGRATING TUBE STAND/ELEV?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VRT TABLE W/INTEGRATING TUBE STAND/ELEV?

The FDA product code for VRT TABLE W/INTEGRATING TUBE STAND/ELEV is KPR.

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 General Electric Co. 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 254 devices →

Related Devices (Code: KPR)

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.

↑