COLLIMATOR MODEL A280BLMD & MODEL A280BLMP
K-Number: K861941 · 1986-07-25
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Device Summary
Frequently Asked Questions
What is the COLLIMATOR MODEL A280BLMD & MODEL A280BLMP?
COLLIMATOR MODEL A280BLMD & MODEL A280BLMP is a medical device that received FDA 510(k) clearance on 1986-07-25. The listed applicant is D&R X-Ray Products, Inc.. The 510(k) number is K861941.
When did COLLIMATOR MODEL A280BLMD & MODEL A280BLMP receive FDA 510(k) clearance?
COLLIMATOR MODEL A280BLMD & MODEL A280BLMP received FDA 510(k) clearance on 1986-07-25, under 510(k) number K861941.
Who is the listed applicant for COLLIMATOR MODEL A280BLMD & MODEL A280BLMP?
The FDA 510(k) record lists D&R X-Ray Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLLIMATOR MODEL A280BLMD & MODEL A280BLMP?
The FDA product code for COLLIMATOR MODEL A280BLMD & MODEL A280BLMP is IZX.
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 D&R X-Ray Products, 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: IZX)
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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