REVERSE-FLOW SYSTEM
K-Number: K834264 · 1984-01-13
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Device Summary
Frequently Asked Questions
What is the REVERSE-FLOW SYSTEM?
REVERSE-FLOW SYSTEM is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Applied Polytechnology, Inc.. The 510(k) number is K834264.
When did REVERSE-FLOW SYSTEM receive FDA 510(k) clearance?
REVERSE-FLOW SYSTEM received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834264.
Who is the listed applicant for REVERSE-FLOW SYSTEM?
The FDA 510(k) record lists Applied Polytechnology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REVERSE-FLOW SYSTEM?
The FDA product code for REVERSE-FLOW SYSTEM is JTA.
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 Applied Polytechnology, 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: JTA)
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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