CRESOLPHTHALEIN COMPLEXONE, CALCIUM
K-Number: K860664 · 1986-06-27
Advertisement
Device Summary
Frequently Asked Questions
What is the CRESOLPHTHALEIN COMPLEXONE, CALCIUM?
CRESOLPHTHALEIN COMPLEXONE, CALCIUM is a medical device that received FDA 510(k) clearance on 1986-06-27. The listed applicant is Amresco, Inc.. The 510(k) number is K860664.
When did CRESOLPHTHALEIN COMPLEXONE, CALCIUM receive FDA 510(k) clearance?
CRESOLPHTHALEIN COMPLEXONE, CALCIUM received FDA 510(k) clearance on 1986-06-27, under 510(k) number K860664.
Who is the listed applicant for CRESOLPHTHALEIN COMPLEXONE, CALCIUM?
The FDA 510(k) record lists Amresco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRESOLPHTHALEIN COMPLEXONE, CALCIUM?
The FDA product code for CRESOLPHTHALEIN COMPLEXONE, CALCIUM is CIC.
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 Amresco, 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: CIC)
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