MOYCO-EDTA
K-Number: K950365 · 1995-04-27
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Device Summary
Frequently Asked Questions
What is the MOYCO-EDTA?
MOYCO-EDTA is a medical device that received FDA 510(k) clearance on 1995-04-27. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. The 510(k) number is K950365.
When did MOYCO-EDTA receive FDA 510(k) clearance?
MOYCO-EDTA received FDA 510(k) clearance on 1995-04-27, under 510(k) number K950365.
Who is the listed applicant for MOYCO-EDTA?
The FDA 510(k) record lists Union Broach, Div. Moyco Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOYCO-EDTA?
The FDA product code for MOYCO-EDTA is KJJ.
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 Union Broach, Div. Moyco Industries, 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: KJJ)
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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