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FDA 510(k)

MANAN MANTA CATHETER FIXATION DISK

K-Number: K954132 · 1996-03-26

ApplicantManan Medical Products, Inc.
Decision Date1996-03-26
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MANAN MANTA CATHETER FIXATION DISK is the device name listed in this FDA 510(k) record. The listed applicant is Manan Medical Products, Inc.. It received FDA 510(k) clearance on 1996-03-26 under 510(k) number K954132. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANAN MANTA CATHETER FIXATION DISK?

MANAN MANTA CATHETER FIXATION DISK is a medical device that received FDA 510(k) clearance on 1996-03-26. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K954132.

When did MANAN MANTA CATHETER FIXATION DISK receive FDA 510(k) clearance?

MANAN MANTA CATHETER FIXATION DISK received FDA 510(k) clearance on 1996-03-26, under 510(k) number K954132.

Who is the listed applicant for MANAN MANTA CATHETER FIXATION DISK?

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

What is the FDA product code for MANAN MANTA CATHETER FIXATION DISK?

The FDA product code for MANAN MANTA CATHETER FIXATION DISK is KNY.

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Other records listing Manan Medical Products, Inc. as applicant

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Related Devices (Code: KNY)

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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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