FDA 510(k)

TRANS/P NEEDLE GUIDE

K-Number: K875236 · 1988-04-15

ApplicantCIVCO Medical Instruments Co., Inc.

Decision Date1988-04-15

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

TRANS/P NEEDLE GUIDE 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 1988-04-15 under 510(k) number K875236. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANS/P NEEDLE GUIDE?

TRANS/P NEEDLE GUIDE is a medical device that received FDA 510(k) clearance on 1988-04-15. The listed applicant is CIVCO Medical Instruments Co., Inc.. The 510(k) number is K875236.

When did TRANS/P NEEDLE GUIDE receive FDA 510(k) clearance?

TRANS/P NEEDLE GUIDE received FDA 510(k) clearance on 1988-04-15, under 510(k) number K875236.

Who is the listed applicant for TRANS/P NEEDLE GUIDE?

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/P NEEDLE GUIDE?

The FDA product code for TRANS/P NEEDLE GUIDE is IYO.

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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.