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FDA 510(k)

INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110

K-Number: K883650 · 1988-09-16

ApplicantInstrumentarium Corp.
Decision Date1988-09-16
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentarium Corp.. It received FDA 510(k) clearance on 1988-09-16 under 510(k) number K883650. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110?

INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110 is a medical device that received FDA 510(k) clearance on 1988-09-16. The listed applicant is Instrumentarium Corp.. The 510(k) number is K883650.

When did INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110 receive FDA 510(k) clearance?

INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110 received FDA 510(k) clearance on 1988-09-16, under 510(k) number K883650.

Who is the listed applicant for INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110?

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

What is the FDA product code for INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110?

The FDA product code for INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110 is LNH.

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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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