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FDA 510(k)

TOSHIBA, SMIT ROENTGEN

K-Number: K870071 · 1987-01-21

ApplicantNorth American Imaging, Inc.
Decision Date1987-01-21
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOSHIBA, SMIT ROENTGEN is the device name listed in this FDA 510(k) record. The listed applicant is North American Imaging, Inc.. It received FDA 510(k) clearance on 1987-01-21 under 510(k) number K870071. 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 TOSHIBA, SMIT ROENTGEN?

TOSHIBA, SMIT ROENTGEN is a medical device that received FDA 510(k) clearance on 1987-01-21. The listed applicant is North American Imaging, Inc.. The 510(k) number is K870071.

When did TOSHIBA, SMIT ROENTGEN receive FDA 510(k) clearance?

TOSHIBA, SMIT ROENTGEN received FDA 510(k) clearance on 1987-01-21, under 510(k) number K870071.

Who is the listed applicant for TOSHIBA, SMIT ROENTGEN?

The FDA 510(k) record lists North American Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOSHIBA, SMIT ROENTGEN?

The FDA product code for TOSHIBA, SMIT ROENTGEN is ITY.

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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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