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FDA 510(k)

DISPOSABLE SHADOW TRAY INSERTS

K-Number: K871215 · 1987-04-06

Decision Date1987-04-06
Product CodeIWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SHADOW TRAY INSERTS is the device name listed in this FDA 510(k) record. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. It received FDA 510(k) clearance on 1987-04-06 under 510(k) number K871215. The device is classified under product code IWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SHADOW TRAY INSERTS?

DISPOSABLE SHADOW TRAY INSERTS is a medical device that received FDA 510(k) clearance on 1987-04-06. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K871215.

When did DISPOSABLE SHADOW TRAY INSERTS receive FDA 510(k) clearance?

DISPOSABLE SHADOW TRAY INSERTS received FDA 510(k) clearance on 1987-04-06, under 510(k) number K871215.

Who is the listed applicant for DISPOSABLE SHADOW TRAY INSERTS?

The FDA 510(k) record lists Mick Radio-Nuclear Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE SHADOW TRAY INSERTS?

The FDA product code for DISPOSABLE SHADOW TRAY INSERTS is IWB.

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 Mick Radio-Nuclear Instruments, 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.

View all 42 devices →

Related Devices (Code: IWB)

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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