MGC/LITTON 2300
K-Number: K820475 · 1982-03-23
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Device Summary
Frequently Asked Questions
What is the MGC/LITTON 2300?
MGC/LITTON 2300 is a medical device that received FDA 510(k) clearance on 1982-03-23. The listed applicant is Medical Graphics Corp.. The 510(k) number is K820475.
When did MGC/LITTON 2300 receive FDA 510(k) clearance?
MGC/LITTON 2300 received FDA 510(k) clearance on 1982-03-23, under 510(k) number K820475.
Who is the listed applicant for MGC/LITTON 2300?
The FDA 510(k) record lists Medical Graphics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MGC/LITTON 2300?
The FDA product code for MGC/LITTON 2300 is BZL.
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 Medical Graphics 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: BZL)
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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