PHYSIOMETRIX CABLE ADAPTER MODIFICATION
K-Number: K935260 · 1993-12-23
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Device Summary
Frequently Asked Questions
What is the PHYSIOMETRIX CABLE ADAPTER MODIFICATION?
PHYSIOMETRIX CABLE ADAPTER MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-12-23. The listed applicant is Physiometrix, Inc.. The 510(k) number is K935260.
When did PHYSIOMETRIX CABLE ADAPTER MODIFICATION receive FDA 510(k) clearance?
PHYSIOMETRIX CABLE ADAPTER MODIFICATION received FDA 510(k) clearance on 1993-12-23, under 510(k) number K935260.
Who is the listed applicant for PHYSIOMETRIX CABLE ADAPTER MODIFICATION?
The FDA 510(k) record lists Physiometrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHYSIOMETRIX CABLE ADAPTER MODIFICATION?
The FDA product code for PHYSIOMETRIX CABLE ADAPTER MODIFICATION is IKD.
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 Physiometrix, 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: IKD)
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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