ACCUDOT 380 SECONDARY I.V. SET
K-Number: K823027 · 1982-11-22
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Device Summary
Frequently Asked Questions
What is the ACCUDOT 380 SECONDARY I.V. SET?
ACCUDOT 380 SECONDARY I.V. SET is a medical device that received FDA 510(k) clearance on 1982-11-22. The listed applicant is Imed Corp.. The 510(k) number is K823027.
When did ACCUDOT 380 SECONDARY I.V. SET receive FDA 510(k) clearance?
ACCUDOT 380 SECONDARY I.V. SET received FDA 510(k) clearance on 1982-11-22, under 510(k) number K823027.
Who is the listed applicant for ACCUDOT 380 SECONDARY I.V. SET?
The FDA 510(k) record lists Imed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCUDOT 380 SECONDARY I.V. SET?
The FDA product code for ACCUDOT 380 SECONDARY I.V. 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.
Other records listing Imed Corp. 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: 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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