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FDA 510(k)

MEDSURG EPIDURAL TRAY/19 GA/BUL TIP/17GA TUO 1002

K-Number: K890731 · 1989-06-23

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

Device Summary

MEDSURG EPIDURAL TRAY/19 GA/BUL TIP/17GA TUO 1002 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 K890731. 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 GA/BUL TIP/17GA TUO 1002?

MEDSURG EPIDURAL TRAY/19 GA/BUL TIP/17GA TUO 1002 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 K890731.

When did MEDSURG EPIDURAL TRAY/19 GA/BUL TIP/17GA TUO 1002 receive FDA 510(k) clearance?

MEDSURG EPIDURAL TRAY/19 GA/BUL TIP/17GA TUO 1002 received FDA 510(k) clearance on 1989-06-23, under 510(k) number K890731.

Who is the listed applicant for MEDSURG EPIDURAL TRAY/19 GA/BUL TIP/17GA TUO 1002?

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 GA/BUL TIP/17GA TUO 1002?

The FDA product code for MEDSURG EPIDURAL TRAY/19 GA/BUL TIP/17GA TUO 1002 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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