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FDA 510(k)

TRANS/R - FP(3)

K-Number: K900016 · 1990-06-11

ApplicantCIVCO Medical Instruments Co., Inc.
Decision Date1990-06-11
Product CodeFCY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRANS/R - FP(3) is the device name listed in this FDA 510(k) record. The listed applicant is CIVCO Medical Instruments Co., Inc.. It received FDA 510(k) clearance on 1990-06-11 under 510(k) number K900016. The device is classified under product code FCY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANS/R - FP(3)?

TRANS/R - FP(3) is a medical device that received FDA 510(k) clearance on 1990-06-11. The listed applicant is CIVCO Medical Instruments Co., Inc.. The 510(k) number is K900016.

When did TRANS/R - FP(3) receive FDA 510(k) clearance?

TRANS/R - FP(3) received FDA 510(k) clearance on 1990-06-11, under 510(k) number K900016.

Who is the listed applicant for TRANS/R - FP(3)?

The FDA 510(k) record lists CIVCO Medical Instruments Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANS/R - FP(3)?

The FDA product code for TRANS/R - FP(3) is FCY.

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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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