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FDA 510(k)

FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER

K-Number: K860605 · 1986-03-24

ApplicantMigada, Ltd.
Decision Date1986-03-24
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Migada, Ltd.. It received FDA 510(k) clearance on 1986-03-24 under 510(k) number K860605. 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 FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER?

FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER is a medical device that received FDA 510(k) clearance on 1986-03-24. The listed applicant is Migada, Ltd.. The 510(k) number is K860605.

When did FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER receive FDA 510(k) clearance?

FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER received FDA 510(k) clearance on 1986-03-24, under 510(k) number K860605.

Who is the listed applicant for FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER?

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 FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER?

The FDA product code for FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER is FPA.

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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.

K943095IV TRANSFER SPIKEK933929LAB-SITE(R) SAFETY CANNULAK902881LAB-SITE SAFETY NEEDLEK870016ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)K864453EMERGENCY & MILITARY INFUSION SYSTEMK863304PRESELECTED FLOW RATE I.V. SET

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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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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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