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FDA 510(k)

PARENTERAL ADMINISTRATION SET

K-Number: K860201 · 1986-02-04

ApplicantMigada, Ltd.
Decision Date1986-02-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PARENTERAL ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Migada, Ltd.. It received FDA 510(k) clearance on 1986-02-04 under 510(k) number K860201. 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 PARENTERAL ADMINISTRATION SET?

PARENTERAL ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1986-02-04. The listed applicant is Migada, Ltd.. The 510(k) number is K860201.

When did PARENTERAL ADMINISTRATION SET receive FDA 510(k) clearance?

PARENTERAL ADMINISTRATION SET received FDA 510(k) clearance on 1986-02-04, under 510(k) number K860201.

Who is the listed applicant for PARENTERAL ADMINISTRATION SET?

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

What is the FDA product code for PARENTERAL ADMINISTRATION SET?

The FDA product code for PARENTERAL ADMINISTRATION 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 Migada, Ltd. 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 15 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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