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FDA 510(k)

CATHETER, SINGLE PUNCTURE Y

K-Number: K770482 · 1977-04-15

ApplicantMdl Medical Device Laboratories, Inc.
Decision Date1977-04-15
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER, SINGLE PUNCTURE Y is the device name listed in this FDA 510(k) record. The listed applicant is Mdl Medical Device Laboratories, Inc.. It received FDA 510(k) clearance on 1977-04-15 under 510(k) number K770482. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, SINGLE PUNCTURE Y?

CATHETER, SINGLE PUNCTURE Y is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Mdl Medical Device Laboratories, Inc.. The 510(k) number is K770482.

When did CATHETER, SINGLE PUNCTURE Y receive FDA 510(k) clearance?

CATHETER, SINGLE PUNCTURE Y received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770482.

Who is the listed applicant for CATHETER, SINGLE PUNCTURE Y?

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

What is the FDA product code for CATHETER, SINGLE PUNCTURE Y?

The FDA product code for CATHETER, SINGLE PUNCTURE Y is KOC.

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Related Devices (Code: KOC)

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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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