RETROGRADE INFUSION SET 3ML & 6ML-
K-Number: K840443 · 1984-04-17
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Device Summary
Frequently Asked Questions
What is the RETROGRADE INFUSION SET 3ML & 6ML-?
RETROGRADE INFUSION SET 3ML & 6ML- is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Tico Medical Instruments, Inc.. The 510(k) number is K840443.
When did RETROGRADE INFUSION SET 3ML & 6ML- receive FDA 510(k) clearance?
RETROGRADE INFUSION SET 3ML & 6ML- received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840443.
Who is the listed applicant for RETROGRADE INFUSION SET 3ML & 6ML-?
The FDA 510(k) record lists Tico Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RETROGRADE INFUSION SET 3ML & 6ML-?
The FDA product code for RETROGRADE INFUSION SET 3ML & 6ML- 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 Tico Medical Instruments, 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: 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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