X-RAY COLLIMATING DEVICES
K-Number: K810598 · 1981-04-10
Advertisement
Device Summary
Frequently Asked Questions
What is the X-RAY COLLIMATING DEVICES?
X-RAY COLLIMATING DEVICES is a medical device that received FDA 510(k) clearance on 1981-04-10. The listed applicant is Midmark Corp.. The 510(k) number is K810598.
When did X-RAY COLLIMATING DEVICES receive FDA 510(k) clearance?
X-RAY COLLIMATING DEVICES received FDA 510(k) clearance on 1981-04-10, under 510(k) number K810598.
Who is the listed applicant for X-RAY COLLIMATING DEVICES?
The FDA 510(k) record lists Midmark Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-RAY COLLIMATING DEVICES?
The FDA product code for X-RAY COLLIMATING DEVICES is IZW.
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 Midmark Corp. 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: IZW)
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