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FDA 510(k)

PERCUTANEOUS GRAINAGE CATHETER

K-Number: K943893 · 1995-03-07

ApplicantMenlo Care, Inc.
Decision Date1995-03-07
Product CodeLJE
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS GRAINAGE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Menlo Care, Inc.. It received FDA 510(k) clearance on 1995-03-07 under 510(k) number K943893. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUTANEOUS GRAINAGE CATHETER?

PERCUTANEOUS GRAINAGE CATHETER is a medical device that received FDA 510(k) clearance on 1995-03-07. The listed applicant is Menlo Care, Inc.. The 510(k) number is K943893.

When did PERCUTANEOUS GRAINAGE CATHETER receive FDA 510(k) clearance?

PERCUTANEOUS GRAINAGE CATHETER received FDA 510(k) clearance on 1995-03-07, under 510(k) number K943893.

Who is the listed applicant for PERCUTANEOUS GRAINAGE CATHETER?

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

What is the FDA product code for PERCUTANEOUS GRAINAGE CATHETER?

The FDA product code for PERCUTANEOUS GRAINAGE CATHETER is LJE.

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Other records listing Menlo Care, Inc. as applicant

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Related Devices (Code: LJE)

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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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