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FDA 510(k)

LILY I.V. SET

K-Number: K884657 · 1989-03-22

Decision Date1989-03-22
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LILY I.V. SET is the device name listed in this FDA 510(k) record. The listed applicant is Modec Co., Inc.. It received FDA 510(k) clearance on 1989-03-22 under 510(k) number K884657. 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 LILY I.V. SET?

LILY I.V. SET is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Modec Co., Inc.. The 510(k) number is K884657.

When did LILY I.V. SET receive FDA 510(k) clearance?

LILY I.V. SET received FDA 510(k) clearance on 1989-03-22, under 510(k) number K884657.

Who is the listed applicant for LILY I.V. SET?

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

What is the FDA product code for LILY I.V. SET?

The FDA product code for LILY I.V. SET is FPA.

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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