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FDA 510(k)

COLLIMATOR MODEL A280BLMD & MODEL A280BLMP

K-Number: K861941 · 1986-07-25

Decision Date1986-07-25
Product CodeIZX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLLIMATOR MODEL A280BLMD & MODEL A280BLMP is the device name listed in this FDA 510(k) record. The listed applicant is D&R X-Ray Products, Inc.. It received FDA 510(k) clearance on 1986-07-25 under 510(k) number K861941. The device is classified under product code IZX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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