TRANSFER SET
K-Number: K923782 · 1993-07-02
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Device Summary
Frequently Asked Questions
What is the TRANSFER SET?
TRANSFER SET is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Pacific Device, Inc.. The 510(k) number is K923782.
When did TRANSFER SET receive FDA 510(k) clearance?
TRANSFER SET received FDA 510(k) clearance on 1993-07-02, under 510(k) number K923782.
Who is the listed applicant for TRANSFER SET?
The FDA 510(k) record lists Pacific Device, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSFER SET?
The FDA product code for TRANSFER SET 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 Pacific Device, 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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