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FDA 510(k)

MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE

K-Number: K852616 · 1986-04-07

Decision Date1986-04-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Hospital Equipment. It received FDA 510(k) clearance on 1986-04-07 under 510(k) number K852616. 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 MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE?

MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE is a medical device that received FDA 510(k) clearance on 1986-04-07. The listed applicant is Medical Hospital Equipment. The 510(k) number is K852616.

When did MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE receive FDA 510(k) clearance?

MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE received FDA 510(k) clearance on 1986-04-07, under 510(k) number K852616.

Who is the listed applicant for MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE?

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

What is the FDA product code for MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE?

The FDA product code for MIRAGE INTRAVENOUS INFUSION SET OLOVSON-STERILE 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 Medical Hospital Equipment 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: 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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