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FDA 510(k)

ANESFLOW-DUAL DRIP IV INFUSION SET

K-Number: K990496 · 1999-07-01

Decision Date1999-07-01
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANESFLOW-DUAL DRIP IV INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Design Assoc.. It received FDA 510(k) clearance on 1999-07-01 under 510(k) number K990496. 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 ANESFLOW-DUAL DRIP IV INFUSION SET?

ANESFLOW-DUAL DRIP IV INFUSION SET is a medical device that received FDA 510(k) clearance on 1999-07-01. The listed applicant is Innovative Design Assoc.. The 510(k) number is K990496.

When did ANESFLOW-DUAL DRIP IV INFUSION SET receive FDA 510(k) clearance?

ANESFLOW-DUAL DRIP IV INFUSION SET received FDA 510(k) clearance on 1999-07-01, under 510(k) number K990496.

Who is the listed applicant for ANESFLOW-DUAL DRIP IV INFUSION SET?

The FDA 510(k) record lists Innovative Design Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESFLOW-DUAL DRIP IV INFUSION SET?

The FDA product code for ANESFLOW-DUAL DRIP IV 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.

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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