STOCKERT 1/4 BUBBLE SENSOR
K-Number: K925541 · 1993-02-02
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Device Summary
Frequently Asked Questions
What is the STOCKERT 1/4 BUBBLE SENSOR?
STOCKERT 1/4 BUBBLE SENSOR is a medical device that received FDA 510(k) clearance on 1993-02-02. The listed applicant is Sorin Biomedica, Fiat, USA, Inc.. The 510(k) number is K925541.
When did STOCKERT 1/4 BUBBLE SENSOR receive FDA 510(k) clearance?
STOCKERT 1/4 BUBBLE SENSOR received FDA 510(k) clearance on 1993-02-02, under 510(k) number K925541.
Who is the listed applicant for STOCKERT 1/4 BUBBLE SENSOR?
The FDA 510(k) record lists Sorin Biomedica, Fiat, USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STOCKERT 1/4 BUBBLE SENSOR?
The FDA product code for STOCKERT 1/4 BUBBLE SENSOR is KRL.
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 Sorin Biomedica, Fiat, USA, 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: KRL)
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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