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FDA 510(k)

HOOK PROBE

K-Number: K854890 · 1986-05-02

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

Device Summary

HOOK PROBE 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 K854890. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOOK PROBE?

HOOK PROBE 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 K854890.

When did HOOK PROBE receive FDA 510(k) clearance?

HOOK PROBE received FDA 510(k) clearance on 1986-05-02, under 510(k) number K854890.

Who is the listed applicant for HOOK PROBE?

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 HOOK PROBE?

The FDA product code for HOOK PROBE is KDC.

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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 FORCEPK854901PACIFIC GRASPERK854891KNIFE

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Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, 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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