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FDA 510(k)

INFUSION STAND

K-Number: K872729 · 1987-07-23

ApplicantCamtec
Decision Date1987-07-23
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSION STAND is the device name listed in this FDA 510(k) record. The listed applicant is Camtec. It received FDA 510(k) clearance on 1987-07-23 under 510(k) number K872729. The device is classified under product code FOX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSION STAND?

INFUSION STAND is a medical device that received FDA 510(k) clearance on 1987-07-23. The listed applicant is Camtec. The 510(k) number is K872729.

When did INFUSION STAND receive FDA 510(k) clearance?

INFUSION STAND received FDA 510(k) clearance on 1987-07-23, under 510(k) number K872729.

Who is the listed applicant for INFUSION STAND?

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

What is the FDA product code for INFUSION STAND?

The FDA product code for INFUSION STAND is FOX.

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 Camtec 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: FOX)

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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