NEMECTRODYN 8
K-Number: K802804 · 1981-03-16
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Device Summary
Frequently Asked Questions
What is the NEMECTRODYN 8?
NEMECTRODYN 8 is a medical device that received FDA 510(k) clearance on 1981-03-16. The listed applicant is Nemectron Medical, Inc.. The 510(k) number is K802804.
When did NEMECTRODYN 8 receive FDA 510(k) clearance?
NEMECTRODYN 8 received FDA 510(k) clearance on 1981-03-16, under 510(k) number K802804.
Who is the listed applicant for NEMECTRODYN 8?
The FDA 510(k) record lists Nemectron Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEMECTRODYN 8?
The FDA product code for NEMECTRODYN 8 is IPF.
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 Nemectron Medical, 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: IPF)
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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