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FDA 510(k)

LARYNGOSCOPE BLADES

K-Number: K883414 · 1988-08-19

ApplicantTruphatek, Ltd.
Decision Date1988-08-19
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSCOPE BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Truphatek, Ltd.. It received FDA 510(k) clearance on 1988-08-19 under 510(k) number K883414. 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 BLADES?

LARYNGOSCOPE BLADES is a medical device that received FDA 510(k) clearance on 1988-08-19. The listed applicant is Truphatek, Ltd.. The 510(k) number is K883414.

When did LARYNGOSCOPE BLADES receive FDA 510(k) clearance?

LARYNGOSCOPE BLADES received FDA 510(k) clearance on 1988-08-19, under 510(k) number K883414.

Who is the listed applicant for LARYNGOSCOPE BLADES?

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

What is the FDA product code for LARYNGOSCOPE BLADES?

The FDA product code for LARYNGOSCOPE BLADES is CCW.

Related Clinical Trials

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Other records listing Truphatek, Ltd. 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.

K923227THROAT-A-SCOPEK920272ORIELK902205OTOSCOPE

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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