TRANSDUCER PROTECTOR
K-Number: K901409 · 1990-07-27
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Device Summary
Frequently Asked Questions
What is the TRANSDUCER PROTECTOR?
TRANSDUCER PROTECTOR is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Filtertek, Inc.. The 510(k) number is K901409.
When did TRANSDUCER PROTECTOR receive FDA 510(k) clearance?
TRANSDUCER PROTECTOR received FDA 510(k) clearance on 1990-07-27, under 510(k) number K901409.
Who is the listed applicant for TRANSDUCER PROTECTOR?
The FDA 510(k) record lists Filtertek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSDUCER PROTECTOR?
The FDA product code for TRANSDUCER PROTECTOR is FIB.
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 Filtertek, 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: FIB)
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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