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FDA 510(k)

MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012

K-Number: K890733 · 1989-06-23

ApplicantMedsurg Industries, Inc.
Decision Date1989-06-23
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012 is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K890733. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012?

MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012 is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K890733.

When did MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012 receive FDA 510(k) clearance?

MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012 received FDA 510(k) clearance on 1989-06-23, under 510(k) number K890733.

Who is the listed applicant for MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012?

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

What is the FDA product code for MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012?

The FDA product code for MEDSURG EPIDURAL TRAY/19 GAGE OPEN END TUOHY 1012 is CAZ.

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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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