S & W SW52E W/POWER BACK LIFT
K-Number: K832768 · 1983-09-20
Advertisement
Device Summary
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.
Advertisement