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FDA 510(k)

LES RAD FILTER

K-Number: K871227 · 1987-06-29

ApplicantM. D. Products
Decision Date1987-06-29
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LES RAD FILTER is the device name listed in this FDA 510(k) record. The listed applicant is M. D. Products. It received FDA 510(k) clearance on 1987-06-29 under 510(k) number K871227. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LES RAD FILTER?

LES RAD FILTER is a medical device that received FDA 510(k) clearance on 1987-06-29. The listed applicant is M. D. Products. The 510(k) number is K871227.

When did LES RAD FILTER receive FDA 510(k) clearance?

LES RAD FILTER received FDA 510(k) clearance on 1987-06-29, under 510(k) number K871227.

Who is the listed applicant for LES RAD FILTER?

The FDA 510(k) record lists M. D. Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LES RAD FILTER?

The FDA product code for LES RAD FILTER is ITY.

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.

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Other records listing M. D. Products 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.

K902948COMFORTRON II (TENS)K884586COMFORTRON DENTAL ANESTHESIA APPARATUS

Related Devices (Code: ITY)

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.

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.

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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