2P-QDA FOOT PRESSURE SYSTEMS REAL TIME
K-Number: K882139 · 1988-06-22
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Device Summary
Frequently Asked Questions
What is the 2P-QDA FOOT PRESSURE SYSTEMS REAL TIME?
2P-QDA FOOT PRESSURE SYSTEMS REAL TIME is a medical device that received FDA 510(k) clearance on 1988-06-22. The listed applicant is Human Performance Technologies, Inc.. The 510(k) number is K882139.
When did 2P-QDA FOOT PRESSURE SYSTEMS REAL TIME receive FDA 510(k) clearance?
2P-QDA FOOT PRESSURE SYSTEMS REAL TIME received FDA 510(k) clearance on 1988-06-22, under 510(k) number K882139.
Who is the listed applicant for 2P-QDA FOOT PRESSURE SYSTEMS REAL TIME?
The FDA 510(k) record lists Human Performance Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 2P-QDA FOOT PRESSURE SYSTEMS REAL TIME?
The FDA product code for 2P-QDA FOOT PRESSURE SYSTEMS REAL TIME is JFC.
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 Human Performance Technologies, 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: JFC)
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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