LILY I.V. SET
K-Number: K884657 · 1989-03-22
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Device Summary
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
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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