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FDA 510(k)

SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS

K-Number: K040870 · 2004-05-17

ApplicantShimadzu Corp.
Decision Date2004-05-17
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corp.. It received FDA 510(k) clearance on 2004-05-17 under 510(k) number K040870. 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 SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS?

SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS is a medical device that received FDA 510(k) clearance on 2004-05-17. The listed applicant is Shimadzu Corp.. The 510(k) number is K040870.

When did SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS receive FDA 510(k) clearance?

SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS received FDA 510(k) clearance on 2004-05-17, under 510(k) number K040870.

Who is the listed applicant for SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS?

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

What is the FDA product code for SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS?

The FDA product code for SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS is JAA.

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Related Devices (Code: 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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