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FDA 510(k)

STOMACH EVACULATOR - EWALD STYLE

K-Number: K864963 · 1987-10-14

ApplicantMedovations, Inc.
Decision Date1987-10-14
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STOMACH EVACULATOR - EWALD STYLE is the device name listed in this FDA 510(k) record. The listed applicant is Medovations, Inc.. It received FDA 510(k) clearance on 1987-10-14 under 510(k) number K864963. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOMACH EVACULATOR - EWALD STYLE?

STOMACH EVACULATOR - EWALD STYLE is a medical device that received FDA 510(k) clearance on 1987-10-14. The listed applicant is Medovations, Inc.. The 510(k) number is K864963.

When did STOMACH EVACULATOR - EWALD STYLE receive FDA 510(k) clearance?

STOMACH EVACULATOR - EWALD STYLE received FDA 510(k) clearance on 1987-10-14, under 510(k) number K864963.

Who is the listed applicant for STOMACH EVACULATOR - EWALD STYLE?

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

What is the FDA product code for STOMACH EVACULATOR - EWALD STYLE?

The FDA product code for STOMACH EVACULATOR - EWALD STYLE is KOA.

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Other records listing Medovations, Inc. 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.

K002363MEDOVATIONS ESOPHAGEAL DILATORK972119MALONEY BOUGE (1210-XX)/HURST BOUGIE (1212-XX)K924646OVER THE GUIDEWIRE DILATATION SYSTEMK913678TROCAR CATHETERK905478YANKAUER SUCTION DEVICEK874309URETHAL CATHETER

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Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, 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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