SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL
K-Number: K983139 · 1999-02-19
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Device Summary
Frequently Asked Questions
What is the SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL?
SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL is a medical device that received FDA 510(k) clearance on 1999-02-19. The listed applicant is GE Medical Systems. The 510(k) number is K983139.
When did SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL receive FDA 510(k) clearance?
SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL received FDA 510(k) clearance on 1999-02-19, under 510(k) number K983139.
Who is the listed applicant for SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL?
The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL?
The FDA product code for SIGNA 1.5T PHOSPHORUS (P) TRANSMIT/RECEIVE FLEX COIL is MOS.
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 GE Medical Systems 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: MOS)
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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