SANITAS PATIENT LIFT
K-Number: K930625 · 1993-09-13
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Device Summary
Frequently Asked Questions
What is the SANITAS PATIENT LIFT?
SANITAS PATIENT LIFT is a medical device that received FDA 510(k) clearance on 1993-09-13. The listed applicant is Dutton-Lainson Co.. The 510(k) number is K930625.
When did SANITAS PATIENT LIFT receive FDA 510(k) clearance?
SANITAS PATIENT LIFT received FDA 510(k) clearance on 1993-09-13, under 510(k) number K930625.
Who is the listed applicant for SANITAS PATIENT LIFT?
The FDA 510(k) record lists Dutton-Lainson Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SANITAS PATIENT LIFT?
The FDA product code for SANITAS PATIENT LIFT is FSA.
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 Dutton-Lainson 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.
Related Devices (Code: FSA)
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.
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