AMWA TDA THEOPHYLLINE TEST
K-Number: K831514 · 1983-06-30
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Device Summary
Frequently Asked Questions
What is the AMWA TDA THEOPHYLLINE TEST?
AMWA TDA THEOPHYLLINE TEST is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K831514.
When did AMWA TDA THEOPHYLLINE TEST receive FDA 510(k) clearance?
AMWA TDA THEOPHYLLINE TEST received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831514.
Who is the listed applicant for AMWA TDA THEOPHYLLINE TEST?
The FDA 510(k) record lists Miles Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMWA TDA THEOPHYLLINE TEST?
The FDA product code for AMWA TDA THEOPHYLLINE TEST is LER.
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.
Other records listing Miles Laboratories, Inc. 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.
Related Devices (Code: LER)
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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