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FDA 510(k)

ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG

K-Number: K891032 · 1989-03-22

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-03-22
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG 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 1989-03-22 under 510(k) number K891032. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG?

ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891032.

When did ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG receive FDA 510(k) clearance?

ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG received FDA 510(k) clearance on 1989-03-22, under 510(k) number K891032.

Who is the listed applicant for ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG?

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 ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG?

The FDA product code for ENDO CERVICAL CURETTE - EVANS, RANDALL, GUSBERG is HHT.

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Related Devices (Code: HHT)

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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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