B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER
K-Number: K883699 · 1988-10-31
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Device Summary
Frequently Asked Questions
What is the B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER?
B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER is a medical device that received FDA 510(k) clearance on 1988-10-31. The listed applicant is Fonar Corp.. The 510(k) number is K883699.
When did B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER receive FDA 510(k) clearance?
B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER received FDA 510(k) clearance on 1988-10-31, under 510(k) number K883699.
Who is the listed applicant for B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER?
The FDA 510(k) record lists Fonar Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER?
The FDA product code for B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER is LNH.
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 Fonar Corp. 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: LNH)
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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