INTRALIG
K-Number: K823536 · 1982-12-28
Advertisement
Device Summary
Frequently Asked Questions
What is the INTRALIG?
INTRALIG is a medical device that received FDA 510(k) clearance on 1982-12-28. The listed applicant is Miltex Instrument Co.. The 510(k) number is K823536.
When did INTRALIG receive FDA 510(k) clearance?
INTRALIG received FDA 510(k) clearance on 1982-12-28, under 510(k) number K823536.
Who is the listed applicant for INTRALIG?
The FDA 510(k) record lists Miltex Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRALIG?
The FDA product code for INTRALIG is EJI.
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 Miltex Instrument Co. 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: EJI)
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