OMNISTIM II COMBIN. THERAPY SYS
K-Number: K843351 · 1984-09-18
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Device Summary
Frequently Asked Questions
What is the OMNISTIM II COMBIN. THERAPY SYS?
OMNISTIM II COMBIN. THERAPY SYS is a medical device that received FDA 510(k) clearance on 1984-09-18. The listed applicant is Physio Technology, Inc.. The 510(k) number is K843351.
When did OMNISTIM II COMBIN. THERAPY SYS receive FDA 510(k) clearance?
OMNISTIM II COMBIN. THERAPY SYS received FDA 510(k) clearance on 1984-09-18, under 510(k) number K843351.
Who is the listed applicant for OMNISTIM II COMBIN. THERAPY SYS?
The FDA 510(k) record lists Physio Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMNISTIM II COMBIN. THERAPY SYS?
The FDA product code for OMNISTIM II COMBIN. THERAPY SYS is IMG.
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 Physio Technology, 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: IMG)
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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