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FDA 510(k)

J&J SCALP VEIN INFUSION SETS

K-Number: K875177 · 1988-01-14

ApplicantCritikon Company, LLC
Decision Date1988-01-14
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

J&J SCALP VEIN INFUSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Critikon Company, LLC. It received FDA 510(k) clearance on 1988-01-14 under 510(k) number K875177. 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 J&J SCALP VEIN INFUSION SETS?

J&J SCALP VEIN INFUSION SETS is a medical device that received FDA 510(k) clearance on 1988-01-14. The listed applicant is Critikon Company, LLC. The 510(k) number is K875177.

When did J&J SCALP VEIN INFUSION SETS receive FDA 510(k) clearance?

J&J SCALP VEIN INFUSION SETS received FDA 510(k) clearance on 1988-01-14, under 510(k) number K875177.

Who is the listed applicant for J&J SCALP VEIN INFUSION SETS?

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

What is the FDA product code for J&J SCALP VEIN INFUSION SETS?

The FDA product code for J&J SCALP VEIN INFUSION SETS is FOZ.

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Other records listing Critikon Company, LLC as applicant

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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

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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