FDA 510(k)

AEGIS I.V. STRIPS

K-Number: K812080 · 1981-08-03

Decision Date1981-08-03

Product CodeKMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

AEGIS I.V. STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1981-08-03 under 510(k) number K812080. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEGIS I.V. STRIPS?

AEGIS I.V. STRIPS is a medical device that received FDA 510(k) clearance on 1981-08-03. The listed applicant is Warner-Lambert Co.. The 510(k) number is K812080.

When did AEGIS I.V. STRIPS receive FDA 510(k) clearance?

AEGIS I.V. STRIPS received FDA 510(k) clearance on 1981-08-03, under 510(k) number K812080.

Who is the listed applicant for AEGIS I.V. STRIPS?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AEGIS I.V. STRIPS?

The FDA product code for AEGIS I.V. STRIPS is KMK.

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Other records listing Warner-Lambert Co. as applicant

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Related Devices (Code: KMK)

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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.