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FDA 510(k)

NORFOLK MEDICAL BUTTERFLY INFUSION SET

K-Number: K870188 · 1987-02-10

Decision Date1987-02-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NORFOLK MEDICAL BUTTERFLY INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Medical Products, Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K870188. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORFOLK MEDICAL BUTTERFLY INFUSION SET?

NORFOLK MEDICAL BUTTERFLY INFUSION SET is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K870188.

When did NORFOLK MEDICAL BUTTERFLY INFUSION SET receive FDA 510(k) clearance?

NORFOLK MEDICAL BUTTERFLY INFUSION SET received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870188.

Who is the listed applicant for NORFOLK MEDICAL BUTTERFLY INFUSION SET?

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

What is the FDA product code for NORFOLK MEDICAL BUTTERFLY INFUSION SET?

The FDA product code for NORFOLK MEDICAL BUTTERFLY INFUSION SET is FPA.

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 Norfolk Medical Products, 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.

View all 20 devices →

Related Devices (Code: FPA)

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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