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FDA 510(k)

SILICONE CATHETER REPAIR KITS

K-Number: K926374 · 1994-10-07

ApplicantAkcess Medical Products, Inc.
Decision Date1994-10-07
Product CodeKOC
Advisory CommitteeGU
DecisionUnknown

Device Summary

SILICONE CATHETER REPAIR KITS is the device name listed in this FDA 510(k) record. The listed applicant is Akcess Medical Products, Inc.. It received FDA 510(k) clearance on 1994-10-07 under 510(k) number K926374. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SILICONE CATHETER REPAIR KITS?

SILICONE CATHETER REPAIR KITS is a medical device that received FDA 510(k) clearance on 1994-10-07. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K926374.

When did SILICONE CATHETER REPAIR KITS receive FDA 510(k) clearance?

SILICONE CATHETER REPAIR KITS received FDA 510(k) clearance on 1994-10-07, under 510(k) number K926374.

Who is the listed applicant for SILICONE CATHETER REPAIR KITS?

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

What is the FDA product code for SILICONE CATHETER REPAIR KITS?

The FDA product code for SILICONE CATHETER REPAIR KITS is KOC.

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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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