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FDA 510(k)

TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.)

K-Number: K993038 · 1999-10-07

ApplicantToshiba America Medical Systems, In.C
Decision Date1999-10-07
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.) is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1999-10-07 under 510(k) number K993038. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.)?

TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.) is a medical device that received FDA 510(k) clearance on 1999-10-07. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K993038.

When did TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.) receive FDA 510(k) clearance?

TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.) received FDA 510(k) clearance on 1999-10-07, under 510(k) number K993038.

Who is the listed applicant for TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.)?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.)?

The FDA product code for TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.) is JAA.

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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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