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FDA 510(k)

I.V. SET WITH AND WITHOUT AIR VENT

K-Number: K860952 · 1986-08-27

ApplicantMigada, Ltd.
Decision Date1986-08-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. SET WITH AND WITHOUT AIR VENT is the device name listed in this FDA 510(k) record. The listed applicant is Migada, Ltd.. It received FDA 510(k) clearance on 1986-08-27 under 510(k) number K860952. 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 I.V. SET WITH AND WITHOUT AIR VENT?

I.V. SET WITH AND WITHOUT AIR VENT is a medical device that received FDA 510(k) clearance on 1986-08-27. The listed applicant is Migada, Ltd.. The 510(k) number is K860952.

When did I.V. SET WITH AND WITHOUT AIR VENT receive FDA 510(k) clearance?

I.V. SET WITH AND WITHOUT AIR VENT received FDA 510(k) clearance on 1986-08-27, under 510(k) number K860952.

Who is the listed applicant for I.V. SET WITH AND WITHOUT AIR VENT?

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 I.V. SET WITH AND WITHOUT AIR VENT?

The FDA product code for I.V. SET WITH AND WITHOUT AIR VENT 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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