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FDA 510(k)

PIM 1.0 LASER DOPPLER PERFUSION IMAGER

K-Number: K920844 · 1992-07-21

ApplicantLisca Development AB
Decision Date1992-07-21
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PIM 1.0 LASER DOPPLER PERFUSION IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is Lisca Development AB. It received FDA 510(k) clearance on 1992-07-21 under 510(k) number K920844. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIM 1.0 LASER DOPPLER PERFUSION IMAGER?

PIM 1.0 LASER DOPPLER PERFUSION IMAGER is a medical device that received FDA 510(k) clearance on 1992-07-21. The listed applicant is Lisca Development AB. The 510(k) number is K920844.

When did PIM 1.0 LASER DOPPLER PERFUSION IMAGER receive FDA 510(k) clearance?

PIM 1.0 LASER DOPPLER PERFUSION IMAGER received FDA 510(k) clearance on 1992-07-21, under 510(k) number K920844.

Who is the listed applicant for PIM 1.0 LASER DOPPLER PERFUSION IMAGER?

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

What is the FDA product code for PIM 1.0 LASER DOPPLER PERFUSION IMAGER?

The FDA product code for PIM 1.0 LASER DOPPLER PERFUSION IMAGER is DPW.

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Official Source

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