IBT MODEL SVI
K-Number: K921821 · 1992-11-02
Advertisement
Device Summary
Frequently Asked Questions
What is the IBT MODEL SVI?
IBT MODEL SVI is a medical device that received FDA 510(k) clearance on 1992-11-02. The listed applicant is Biomagnetic Technologies, Inc.. The 510(k) number is K921821.
When did IBT MODEL SVI receive FDA 510(k) clearance?
IBT MODEL SVI received FDA 510(k) clearance on 1992-11-02, under 510(k) number K921821.
Who is the listed applicant for IBT MODEL SVI?
The FDA 510(k) record lists Biomagnetic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IBT MODEL SVI?
The FDA product code for IBT MODEL SVI is CBK.
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 Biomagnetic Technologies, 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: CBK)
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.
Advertisement