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FDA 510(k)

VENTED NEEDLE

K-Number: K932462 · 1993-09-15

Decision Date1993-09-15
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENTED NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Excel Medical, Inc.. It received FDA 510(k) clearance on 1993-09-15 under 510(k) number K932462. 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 VENTED NEEDLE?

VENTED NEEDLE is a medical device that received FDA 510(k) clearance on 1993-09-15. The listed applicant is Excel Medical, Inc.. The 510(k) number is K932462.

When did VENTED NEEDLE receive FDA 510(k) clearance?

VENTED NEEDLE received FDA 510(k) clearance on 1993-09-15, under 510(k) number K932462.

Who is the listed applicant for VENTED NEEDLE?

The FDA 510(k) record lists Excel Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTED NEEDLE?

The FDA product code for VENTED NEEDLE 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 Excel Medical, 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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