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FDA 510(k)

NOVY CORNUAL CANNULATION SET

K-Number: K931476 · 1995-07-28

ApplicantCook Ob/Gyn
Decision Date1995-07-28
Product CodeMOV
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NOVY CORNUAL CANNULATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1995-07-28 under 510(k) number K931476. The device is classified under product code MOV. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVY CORNUAL CANNULATION SET?

NOVY CORNUAL CANNULATION SET is a medical device that received FDA 510(k) clearance on 1995-07-28. The listed applicant is Cook Ob/Gyn. The 510(k) number is K931476.

When did NOVY CORNUAL CANNULATION SET receive FDA 510(k) clearance?

NOVY CORNUAL CANNULATION SET received FDA 510(k) clearance on 1995-07-28, under 510(k) number K931476.

Who is the listed applicant for NOVY CORNUAL CANNULATION SET?

The FDA 510(k) record lists Cook Ob/Gyn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOVY CORNUAL CANNULATION SET?

The FDA product code for NOVY CORNUAL CANNULATION SET is MOV.

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Other records listing Cook Ob/Gyn as applicant

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.

K062438BAKRI POSTPARTUM BALLOON, MODEL J-SOS-100500K030441SYDNEY IVF BLASTOCYST CRYOPRESERVATION KIT AND SYDNEY IVF BLASTOCYST THAW KITK023850SYDNEY IVF EMBRYO BIOPSY MEDIUMK013597TAMPONADE UTERINE BALLOON CATHETER SETK002385COOK IVF FOLLICLE FLUSHING BUFFER, COOK IVF OOCYTE WASH BUFFER, COOK IVF FERTILIZATION MEDIUM, COOK IVF CLEAVAGE MEDIUM,K002383COOK IVF SPERM BUFFER, COOK IVF SPERM MEDIUM, AND COOK IVF SPERM GRADIENT KIT

View all 43 devices →

Related Devices (Code: MOV)

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.

K180552Modified Novy Cornual Cannulation SetCook IncorporatedK932436ECHOMARK INTRAUTERINE GUIDING CATHETEREchocath, Inc.K931534OVAMED INTRAUTERINE ACCESS CATHETEROvamed Corp.K953314CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEMConceptus, Inc.

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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