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FDA 510(k)

UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET

K-Number: K891028 · 1989-03-17

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-03-17
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET 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 1989-03-17 under 510(k) number K891028. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET?

UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET is a medical device that received FDA 510(k) clearance on 1989-03-17. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891028.

When did UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET receive FDA 510(k) clearance?

UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET received FDA 510(k) clearance on 1989-03-17, under 510(k) number K891028.

Who is the listed applicant for UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET?

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 UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET?

The FDA product code for UTERINE CANNULA - KAHN, JARCO, CORSON, RATCHET is HIG.

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Related Devices (Code: HIG)

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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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