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FDA 510(k)

LARYNGOSCOPE BLADE (ROBERTSHAW STYLE)

K-Number: K884073 · 1988-10-13

ApplicantEastmed Enterprises, Inc.
Decision Date1988-10-13
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSCOPE BLADE (ROBERTSHAW STYLE) is the device name listed in this FDA 510(k) record. The listed applicant is Eastmed Enterprises, Inc.. It received FDA 510(k) clearance on 1988-10-13 under 510(k) number K884073. 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 LARYNGOSCOPE BLADE (ROBERTSHAW STYLE)?

LARYNGOSCOPE BLADE (ROBERTSHAW STYLE) is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is Eastmed Enterprises, Inc.. The 510(k) number is K884073.

When did LARYNGOSCOPE BLADE (ROBERTSHAW STYLE) receive FDA 510(k) clearance?

LARYNGOSCOPE BLADE (ROBERTSHAW STYLE) received FDA 510(k) clearance on 1988-10-13, under 510(k) number K884073.

Who is the listed applicant for LARYNGOSCOPE BLADE (ROBERTSHAW STYLE)?

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

What is the FDA product code for LARYNGOSCOPE BLADE (ROBERTSHAW STYLE)?

The FDA product code for LARYNGOSCOPE BLADE (ROBERTSHAW STYLE) is CCW.

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Other records listing Eastmed Enterprises, 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.

K922019LARYNGOSCOPE RIGIDK921128ENDOTRACHEAL TUBE STYLETK914741AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIEDK903618ROBERTAZZI NASOPHARYNGEAL AIRWAYK901489MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE)K890342AIRWAYS (GUEDEL, BERMAN & NASOPHARYNGEAL TYPES)

View all 13 devices →

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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