SORBA MODEL CIC-1000 W/NEW ELECTRODES
K-Number: K901926 · 1990-06-12
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Device Summary
Frequently Asked Questions
What is the SORBA MODEL CIC-1000 W/NEW ELECTRODES?
SORBA MODEL CIC-1000 W/NEW ELECTRODES is a medical device that received FDA 510(k) clearance on 1990-06-12. The listed applicant is Sorba Medical Systems, Inc.. The 510(k) number is K901926.
When did SORBA MODEL CIC-1000 W/NEW ELECTRODES receive FDA 510(k) clearance?
SORBA MODEL CIC-1000 W/NEW ELECTRODES received FDA 510(k) clearance on 1990-06-12, under 510(k) number K901926.
Who is the listed applicant for SORBA MODEL CIC-1000 W/NEW ELECTRODES?
The FDA 510(k) record lists Sorba Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SORBA MODEL CIC-1000 W/NEW ELECTRODES?
The FDA product code for SORBA MODEL CIC-1000 W/NEW ELECTRODES is DXG.
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 Sorba Medical Systems, 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: DXG)
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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