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FDA 510(k)

OLSEN #770 DISPOSABLE HOLSTER

K-Number: K820158 · 1982-02-05

ApplicantOlsen Electro-Surgical Instruments, Inc.
Decision Date1982-02-05
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OLSEN #770 DISPOSABLE HOLSTER is the device name listed in this FDA 510(k) record. The listed applicant is Olsen Electro-Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820158. 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 OLSEN #770 DISPOSABLE HOLSTER?

OLSEN #770 DISPOSABLE HOLSTER is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Olsen Electro-Surgical Instruments, Inc.. The 510(k) number is K820158.

When did OLSEN #770 DISPOSABLE HOLSTER receive FDA 510(k) clearance?

OLSEN #770 DISPOSABLE HOLSTER received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820158.

Who is the listed applicant for OLSEN #770 DISPOSABLE HOLSTER?

The FDA 510(k) record lists Olsen Electro-Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLSEN #770 DISPOSABLE HOLSTER?

The FDA product code for OLSEN #770 DISPOSABLE HOLSTER is KDC.

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Other records listing Olsen Electro-Surgical Instruments, 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.

K834410DOUBLE-COAGULATION SWITCHPEN 757K834329OLSEN 756 ROCKER SWITCHPEN

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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