TRANSFER-AID(TM)
K-Number: K913985 · 1992-03-18
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Device Summary
Frequently Asked Questions
What is the TRANSFER-AID(TM)?
TRANSFER-AID(TM) is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is Healthtek, Inc.. The 510(k) number is K913985.
When did TRANSFER-AID(TM) receive FDA 510(k) clearance?
TRANSFER-AID(TM) received FDA 510(k) clearance on 1992-03-18, under 510(k) number K913985.
Who is the listed applicant for TRANSFER-AID(TM)?
The FDA 510(k) record lists Healthtek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSFER-AID(TM)?
The FDA product code for TRANSFER-AID(TM) is LHI.
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 Healthtek, 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: LHI)
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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