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FDA 510(k)

CATHETERS, MALE, FEMALE

K-Number: K892691 · 1989-06-23

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-06-23
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETERS, MALE, FEMALE is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K892691. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETERS, MALE, FEMALE?

CATHETERS, MALE, FEMALE is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K892691.

When did CATHETERS, MALE, FEMALE receive FDA 510(k) clearance?

CATHETERS, MALE, FEMALE received FDA 510(k) clearance on 1989-06-23, under 510(k) number K892691.

Who is the listed applicant for CATHETERS, MALE, FEMALE?

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

What is the FDA product code for CATHETERS, MALE, FEMALE?

The FDA product code for CATHETERS, MALE, FEMALE is KOD.

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Related Devices (Code: KOD)

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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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