MAGILL FORCEPS
K-Number: K880319 · 1988-03-21
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Device Summary
Frequently Asked Questions
What is the MAGILL FORCEPS?
MAGILL FORCEPS is a medical device that received FDA 510(k) clearance on 1988-03-21. The listed applicant is Eastmed Enterprises, Inc.. The 510(k) number is K880319.
When did MAGILL FORCEPS receive FDA 510(k) clearance?
MAGILL FORCEPS received FDA 510(k) clearance on 1988-03-21, under 510(k) number K880319.
Who is the listed applicant for MAGILL FORCEPS?
The FDA 510(k) record lists Eastmed Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAGILL FORCEPS?
The FDA product code for MAGILL FORCEPS is BWB.
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 Eastmed Enterprises, 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: BWB)
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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