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FDA 510(k)

D.L. SCOPE BLADE & HANDLE

K-Number: K841778 · 1984-05-23

ApplicantNorth American Medical Products, Inc.
Decision Date1984-05-23
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

D.L. SCOPE BLADE & HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is North American Medical Products, Inc.. It received FDA 510(k) clearance on 1984-05-23 under 510(k) number K841778. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D.L. SCOPE BLADE & HANDLE?

D.L. SCOPE BLADE & HANDLE is a medical device that received FDA 510(k) clearance on 1984-05-23. The listed applicant is North American Medical Products, Inc.. The 510(k) number is K841778.

When did D.L. SCOPE BLADE & HANDLE receive FDA 510(k) clearance?

D.L. SCOPE BLADE & HANDLE received FDA 510(k) clearance on 1984-05-23, under 510(k) number K841778.

Who is the listed applicant for D.L. SCOPE BLADE & HANDLE?

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

What is the FDA product code for D.L. SCOPE BLADE & HANDLE?

The FDA product code for D.L. SCOPE BLADE & HANDLE is CCW.

Related Clinical Trials

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Other records listing North American Medical Products, 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.

K001965SAFE-POINT VAC, SAFE-POINT M-D BLOOD COLLECTION SYSTEMSK905305SAFE-SITE NEEDLE COVERK895948PORT-O-SCOPE(TM)K896072D.L. SCOPE OPHTHALMOSCOPEK862661D.L. SCOPE(R) OTOSCOPE

Related Devices (Code: CCW)

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.

K191602APA Oxy BladeVenner Medical (Singapore) Pte, Ltd.K163412Girgis Scope Video 200 Double Bladed Laryngoscope (GSV200.DBL)Girgis Scope, LLCK121378AIRTRAQ SP AIRTRAQ AVANTProdol Meditec , Ltd.K063477NOVAMED MRI CONDITIONAL LARYNGOSCOPE SETNovamed, LLCK062523TRU-MR LARYNGOSCOPE SETTruphatek International, Ltd.K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002Minrad, 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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