ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP
K-Number: K943287 · 1994-12-27
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Device Summary
Frequently Asked Questions
What is the ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP?
ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is Ndm Acquisition Corp.. The 510(k) number is K943287.
When did ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP receive FDA 510(k) clearance?
ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP received FDA 510(k) clearance on 1994-12-27, under 510(k) number K943287.
Who is the listed applicant for ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP?
The FDA 510(k) record lists Ndm Acquisition Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP?
The FDA product code for ACT-ONE ADVANCED COMPRESSION TECHNOLOGY FOOT PUMP is JOW.
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 Ndm Acquisition 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: JOW)
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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