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FDA 510(k)

TRANSFER SET

K-Number: K923782 · 1993-07-02

Decision Date1993-07-02
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRANSFER SET is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Device, Inc.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K923782. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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