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FDA 510(k)

NORFOLK/NORWICH PRESSURE INFUSION BOX

K-Number: K810954 · 1981-04-21

Decision Date1981-04-21
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NORFOLK/NORWICH PRESSURE INFUSION BOX is the device name listed in this FDA 510(k) record. The listed applicant is Medical Innovations Corp.. It received FDA 510(k) clearance on 1981-04-21 under 510(k) number K810954. The device is classified under product code KZD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORFOLK/NORWICH PRESSURE INFUSION BOX?

NORFOLK/NORWICH PRESSURE INFUSION BOX is a medical device that received FDA 510(k) clearance on 1981-04-21. The listed applicant is Medical Innovations Corp.. The 510(k) number is K810954.

When did NORFOLK/NORWICH PRESSURE INFUSION BOX receive FDA 510(k) clearance?

NORFOLK/NORWICH PRESSURE INFUSION BOX received FDA 510(k) clearance on 1981-04-21, under 510(k) number K810954.

Who is the listed applicant for NORFOLK/NORWICH PRESSURE INFUSION BOX?

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

What is the FDA product code for NORFOLK/NORWICH PRESSURE INFUSION BOX?

The FDA product code for NORFOLK/NORWICH PRESSURE INFUSION BOX is KZD.

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 Medical Innovations Corp. 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.

View all 24 devices →

Related Devices (Code: KZD)

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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