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)

V-1504 VERTICAL PLATFORM LIFT

K-Number: K960739 · 1996-04-01

Decision Date1996-04-01
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

V-1504 VERTICAL PLATFORM LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Barnes,Richardson & Colburn. It received FDA 510(k) clearance on 1996-04-01 under 510(k) number K960739. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-1504 VERTICAL PLATFORM LIFT?

V-1504 VERTICAL PLATFORM LIFT is a medical device that received FDA 510(k) clearance on 1996-04-01. The listed applicant is Barnes,Richardson & Colburn. The 510(k) number is K960739.

When did V-1504 VERTICAL PLATFORM LIFT receive FDA 510(k) clearance?

V-1504 VERTICAL PLATFORM LIFT received FDA 510(k) clearance on 1996-04-01, under 510(k) number K960739.

Who is the listed applicant for V-1504 VERTICAL PLATFORM LIFT?

The FDA 510(k) record lists Barnes,Richardson & Colburn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-1504 VERTICAL PLATFORM LIFT?

The FDA product code for V-1504 VERTICAL PLATFORM LIFT is ING.

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 Barnes,Richardson & Colburn 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: ING)

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.

↑