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FDA 510(k)

MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001

K-Number: K062231 · 2006-08-31

ApplicantMinrad, Inc.
Decision Date2006-08-31
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 is the device name listed in this FDA 510(k) record. The listed applicant is Minrad, Inc.. It received FDA 510(k) clearance on 2006-08-31 under 510(k) number K062231. 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 MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001?

MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 is a medical device that received FDA 510(k) clearance on 2006-08-31. The listed applicant is Minrad, Inc.. The 510(k) number is K062231.

When did MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 receive FDA 510(k) clearance?

MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 received FDA 510(k) clearance on 2006-08-31, under 510(k) number K062231.

Who is the listed applicant for MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001?

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

What is the FDA product code for MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001?

The FDA product code for MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 is CCW.

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Other records listing Minrad, 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.

K072255MINRAD INC. NASAL SCAVENGING CIRCUITK071814LIGHT SABRE SPINAL ACCESS DEVICEK062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002K041852MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002K041846SABRESOURCE DRAPEK021084LIGHT SABER SPINAL NEEDLE

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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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