MAXICEPTOR
K-Number: K780632 · 1978-08-14
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Device Summary
Frequently Asked Questions
What is the MAXICEPTOR?
MAXICEPTOR is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Med General. The 510(k) number is K780632.
When did MAXICEPTOR receive FDA 510(k) clearance?
MAXICEPTOR received FDA 510(k) clearance on 1978-08-14, under 510(k) number K780632.
Who is the listed applicant for MAXICEPTOR?
The FDA 510(k) record lists Med General as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXICEPTOR?
The FDA product code for MAXICEPTOR is ISB.
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 Med General 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: ISB)
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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