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FDA 510(k)

NEEDLELESS INJECTION CANNULA

K-Number: K923653 · 1993-05-13

Decision Date1993-05-13
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLELESS INJECTION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1993-05-13 under 510(k) number K923653. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLELESS INJECTION CANNULA?

NEEDLELESS INJECTION CANNULA is a medical device that received FDA 510(k) clearance on 1993-05-13. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K923653.

When did NEEDLELESS INJECTION CANNULA receive FDA 510(k) clearance?

NEEDLELESS INJECTION CANNULA received FDA 510(k) clearance on 1993-05-13, under 510(k) number K923653.

Who is the listed applicant for NEEDLELESS INJECTION CANNULA?

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

What is the FDA product code for NEEDLELESS INJECTION CANNULA?

The FDA product code for NEEDLELESS INJECTION CANNULA is LJS.

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 Arrow Intl., 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.

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Related Devices (Code: LJS)

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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