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FDA 510(k)

PRC AUTOPSY DEVICE

K-Number: K913536 · 1991-11-22

ApplicantPennstate
Decision Date1991-11-22
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRC AUTOPSY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Pennstate. It received FDA 510(k) clearance on 1991-11-22 under 510(k) number K913536. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRC AUTOPSY DEVICE?

PRC AUTOPSY DEVICE is a medical device that received FDA 510(k) clearance on 1991-11-22. The listed applicant is Pennstate. The 510(k) number is K913536.

When did PRC AUTOPSY DEVICE receive FDA 510(k) clearance?

PRC AUTOPSY DEVICE received FDA 510(k) clearance on 1991-11-22, under 510(k) number K913536.

Who is the listed applicant for PRC AUTOPSY DEVICE?

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

What is the FDA product code for PRC AUTOPSY DEVICE?

The FDA product code for PRC AUTOPSY DEVICE is KKX.

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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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