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FDA 510(k)

LITE-BLADE

K-Number: K944428 · 1994-11-15

ApplicantEare Consulting Service
Decision Date1994-11-15
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LITE-BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Eare Consulting Service. It received FDA 510(k) clearance on 1994-11-15 under 510(k) number K944428. 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 LITE-BLADE?

LITE-BLADE is a medical device that received FDA 510(k) clearance on 1994-11-15. The listed applicant is Eare Consulting Service. The 510(k) number is K944428.

When did LITE-BLADE receive FDA 510(k) clearance?

LITE-BLADE received FDA 510(k) clearance on 1994-11-15, under 510(k) number K944428.

Who is the listed applicant for LITE-BLADE?

The FDA 510(k) record lists Eare Consulting Service as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITE-BLADE?

The FDA product code for LITE-BLADE is CCW.

Related Clinical Trials

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Other records listing Eare Consulting Service 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.

K970180VSA 3000 VIBRATORYN SENSORY ANALYZERK950592ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURESK934981DENTAL DRILL

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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