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FDA 510(k)

INJECTO FLUSH

K-Number: K964120 · 1996-12-30

ApplicantRobert J. Jynch, Jr.
Decision Date1996-12-30
Product CodeFCL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INJECTO FLUSH is the device name listed in this FDA 510(k) record. The listed applicant is Robert J. Jynch, Jr.. It received FDA 510(k) clearance on 1996-12-30 under 510(k) number K964120. The device is classified under product code FCL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTO FLUSH?

INJECTO FLUSH is a medical device that received FDA 510(k) clearance on 1996-12-30. The listed applicant is Robert J. Jynch, Jr.. The 510(k) number is K964120.

When did INJECTO FLUSH receive FDA 510(k) clearance?

INJECTO FLUSH received FDA 510(k) clearance on 1996-12-30, under 510(k) number K964120.

Who is the listed applicant for INJECTO FLUSH?

The FDA 510(k) record lists Robert J. Jynch, Jr. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INJECTO FLUSH?

The FDA product code for INJECTO FLUSH is FCL.

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Related Devices (Code: FCL)

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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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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