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FDA 510(k)

ROSCO PYRR

K-Number: K894221 · 1989-09-28

ApplicantPro-Lab, Inc.
Decision Date1989-09-28
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ROSCO PYRR is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Lab, Inc.. It received FDA 510(k) clearance on 1989-09-28 under 510(k) number K894221. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROSCO PYRR?

ROSCO PYRR is a medical device that received FDA 510(k) clearance on 1989-09-28. The listed applicant is Pro-Lab, Inc.. The 510(k) number is K894221.

When did ROSCO PYRR receive FDA 510(k) clearance?

ROSCO PYRR received FDA 510(k) clearance on 1989-09-28, under 510(k) number K894221.

Who is the listed applicant for ROSCO PYRR?

The FDA 510(k) record lists Pro-Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROSCO PYRR?

The FDA product code for ROSCO PYRR is JTO.

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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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