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FDA 510(k)

LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT

K-Number: K930787 · 1993-07-09

ApplicantAdvanced Surgical, Inc.
Decision Date1993-07-09
Product CodeDQX
Advisory CommitteeCV
DecisionUnknown

Device Summary

LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical, Inc.. It received FDA 510(k) clearance on 1993-07-09 under 510(k) number K930787. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT?

LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K930787.

When did LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT receive FDA 510(k) clearance?

LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT received FDA 510(k) clearance on 1993-07-09, under 510(k) number K930787.

Who is the listed applicant for LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT?

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

What is the FDA product code for LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT?

The FDA product code for LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER KIT is DQX.

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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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