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FDA 510(k)

INJECTION CAP

K-Number: K940775 · 1994-06-15

ApplicantMedron, Inc.
Decision Date1994-06-15
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INJECTION CAP is the device name listed in this FDA 510(k) record. The listed applicant is Medron, Inc.. It received FDA 510(k) clearance on 1994-06-15 under 510(k) number K940775. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTION CAP?

INJECTION CAP is a medical device that received FDA 510(k) clearance on 1994-06-15. The listed applicant is Medron, Inc.. The 510(k) number is K940775.

When did INJECTION CAP receive FDA 510(k) clearance?

INJECTION CAP received FDA 510(k) clearance on 1994-06-15, under 510(k) number K940775.

Who is the listed applicant for INJECTION CAP?

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

What is the FDA product code for INJECTION CAP?

The FDA product code for INJECTION CAP is FOZ.

Related Clinical Trials

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Other records listing Medron, 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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)

Related Devices (Code: FOZ)

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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