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FDA 510(k)

DFI-1000 AND DVS-475 IMAGING DEVICES

K-Number: K951261 · 1996-03-15

ApplicantNical
Decision Date1996-03-15
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DFI-1000 AND DVS-475 IMAGING DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Nical. It received FDA 510(k) clearance on 1996-03-15 under 510(k) number K951261. 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 DFI-1000 AND DVS-475 IMAGING DEVICES?

DFI-1000 AND DVS-475 IMAGING DEVICES is a medical device that received FDA 510(k) clearance on 1996-03-15. The listed applicant is Nical. The 510(k) number is K951261.

When did DFI-1000 AND DVS-475 IMAGING DEVICES receive FDA 510(k) clearance?

DFI-1000 AND DVS-475 IMAGING DEVICES received FDA 510(k) clearance on 1996-03-15, under 510(k) number K951261.

Who is the listed applicant for DFI-1000 AND DVS-475 IMAGING DEVICES?

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

What is the FDA product code for DFI-1000 AND DVS-475 IMAGING DEVICES?

The FDA product code for DFI-1000 AND DVS-475 IMAGING DEVICES is JAA.

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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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