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)

S & W SW52E W/POWER BACK LIFT

K-Number: K832768 · 1983-09-20

Decision Date1983-09-20
Product CodeLGX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

S & W SW52E W/POWER BACK LIFT is the device name listed in this FDA 510(k) record. The listed applicant is S & W Enterprises, Inc.. It received FDA 510(k) clearance on 1983-09-20 under 510(k) number K832768. The device is classified under product code LGX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S & W SW52E W/POWER BACK LIFT?

S & W SW52E W/POWER BACK LIFT is a medical device that received FDA 510(k) clearance on 1983-09-20. The listed applicant is S & W Enterprises, Inc.. The 510(k) number is K832768.

When did S & W SW52E W/POWER BACK LIFT receive FDA 510(k) clearance?

S & W SW52E W/POWER BACK LIFT received FDA 510(k) clearance on 1983-09-20, under 510(k) number K832768.

Who is the listed applicant for S & W SW52E W/POWER BACK LIFT?

The FDA 510(k) record lists S & W Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for S & W SW52E W/POWER BACK LIFT?

The FDA product code for S & W SW52E W/POWER BACK LIFT is LGX.

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 S & W Enterprises, Inc. 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: LGX)

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.

↑