PHYNE-TOUCH PF
K-Number: K931250 · 1994-01-28
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Device Summary
Frequently Asked Questions
What is the PHYNE-TOUCH PF?
PHYNE-TOUCH PF is a medical device that received FDA 510(k) clearance on 1994-01-28. The listed applicant is Medical Resources, Ltd.. The 510(k) number is K931250.
When did PHYNE-TOUCH PF receive FDA 510(k) clearance?
PHYNE-TOUCH PF received FDA 510(k) clearance on 1994-01-28, under 510(k) number K931250.
Who is the listed applicant for PHYNE-TOUCH PF?
The FDA 510(k) record lists Medical Resources, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHYNE-TOUCH PF?
The FDA product code for PHYNE-TOUCH PF is LYY.
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 Medical Resources, Ltd. 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: LYY)
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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