ET - EXTENSION SETS
K-Number: K853387 · 1985-08-22
Advertisement
Device Summary
Frequently Asked Questions
What is the ET - EXTENSION SETS?
ET - EXTENSION SETS is a medical device that received FDA 510(k) clearance on 1985-08-22. The listed applicant is Migada, Ltd.. The 510(k) number is K853387.
When did ET - EXTENSION SETS receive FDA 510(k) clearance?
ET - EXTENSION SETS received FDA 510(k) clearance on 1985-08-22, under 510(k) number K853387.
Who is the listed applicant for ET - EXTENSION SETS?
The FDA 510(k) record lists Migada, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ET - EXTENSION SETS?
The FDA product code for ET - EXTENSION SETS is FPA.
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 Migada, Ltd. 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: FPA)
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.
Advertisement