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FDA 510(k)

KNIFE

K-Number: K854891 · 1986-05-02

ApplicantEuro-Med Intl.
Decision Date1986-05-02
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Euro-Med Intl.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K854891. The device is classified under product code EMF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNIFE?

KNIFE is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Euro-Med Intl.. The 510(k) number is K854891.

When did KNIFE receive FDA 510(k) clearance?

KNIFE received FDA 510(k) clearance on 1986-05-02, under 510(k) number K854891.

Who is the listed applicant for KNIFE?

The FDA 510(k) record lists Euro-Med Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KNIFE?

The FDA product code for KNIFE is EMF.

Related Clinical Trials

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Other records listing Euro-Med Intl. 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.

K883884PROSTATIC CORE-CUT NEEDLEK882404KEVOR-CURETTEK854897MAX-I-GRASPK854895BASKET FORCEPK854890HOOK PROBEK854901PACIFIC GRASPER

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Related Devices (Code: EMF)

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.

K080133MOUNTABLE ENDOSCOPIC BLADEA.M. Surgical, Inc.K982142MOUNTABLE ENDOSCOPIC KNIFEA.M. Surgical, Inc.K890217MICROSURGICAL KNIVESKinetic Medical ProductsK890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890214MICROSURGERY RAZOR BLADE HOLDERKinetic Medical ProductsK880094VAN-TEC ENDOPYELOTOMY KNIFEVan-Tec, 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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