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FDA 510(k)

IVORY FINDER SET

K-Number: K881794 · 1988-07-08

ApplicantIvory Instruments Co.
Decision Date1988-07-08
Product CodeHCY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

IVORY FINDER SET is the device name listed in this FDA 510(k) record. The listed applicant is Ivory Instruments Co.. It received FDA 510(k) clearance on 1988-07-08 under 510(k) number K881794. The device is classified under product code HCY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IVORY FINDER SET?

IVORY FINDER SET is a medical device that received FDA 510(k) clearance on 1988-07-08. The listed applicant is Ivory Instruments Co.. The 510(k) number is K881794.

When did IVORY FINDER SET receive FDA 510(k) clearance?

IVORY FINDER SET received FDA 510(k) clearance on 1988-07-08, under 510(k) number K881794.

Who is the listed applicant for IVORY FINDER SET?

The FDA 510(k) record lists Ivory Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IVORY FINDER SET?

The FDA product code for IVORY FINDER SET is HCY.

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Related Devices (Code: HCY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K980096OAC (OPTICAL ASPIRATING CURETTE)Imagyn Medical Technologies, Inc.K944238ENDOCYTE TMD.L. Nelson and Assoc., Inc.K935822PHASE I CURETTEPhase I Corp.K901442BAXTER D & C TRAYBaxter Healthcare CorpK890384UTERINE CURETTEKinetic Medical ProductsK862297THE D & C PAD-SACNu-Gyn-Tek, Inc.

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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