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FDA 510(k)

MILL ROSE ERCP CANNULAS

K-Number: K941401 · 1994-08-17

ApplicantMill-Rose Lab, Inc.
Decision Date1994-08-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MILL ROSE ERCP CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Mill-Rose Lab, Inc.. It received FDA 510(k) clearance on 1994-08-17 under 510(k) number K941401. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILL ROSE ERCP CANNULAS?

MILL ROSE ERCP CANNULAS is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Mill-Rose Lab, Inc.. The 510(k) number is K941401.

When did MILL ROSE ERCP CANNULAS receive FDA 510(k) clearance?

MILL ROSE ERCP CANNULAS received FDA 510(k) clearance on 1994-08-17, under 510(k) number K941401.

Who is the listed applicant for MILL ROSE ERCP CANNULAS?

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

What is the FDA product code for MILL ROSE ERCP CANNULAS?

The FDA product code for MILL ROSE ERCP CANNULAS is GCJ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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