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FDA 510(k)

FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000)

K-Number: K883519 · 1988-10-19

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1988-10-19
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000) is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1988-10-19 under 510(k) number K883519. 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 FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000)?

FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000) is a medical device that received FDA 510(k) clearance on 1988-10-19. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K883519.

When did FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000) receive FDA 510(k) clearance?

FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000) received FDA 510(k) clearance on 1988-10-19, under 510(k) number K883519.

Who is the listed applicant for FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000)?

The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000)?

The FDA product code for FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000) 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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