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FDA 510(k)

LIGHT SABER INTRODUCER NEEDLE

K-Number: K013040 · 2001-12-07

ApplicantMinrad, Inc.
Decision Date2001-12-07
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHT SABER INTRODUCER NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Minrad, Inc.. It received FDA 510(k) clearance on 2001-12-07 under 510(k) number K013040. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT SABER INTRODUCER NEEDLE?

LIGHT SABER INTRODUCER NEEDLE is a medical device that received FDA 510(k) clearance on 2001-12-07. The listed applicant is Minrad, Inc.. The 510(k) number is K013040.

When did LIGHT SABER INTRODUCER NEEDLE receive FDA 510(k) clearance?

LIGHT SABER INTRODUCER NEEDLE received FDA 510(k) clearance on 2001-12-07, under 510(k) number K013040.

Who is the listed applicant for LIGHT SABER INTRODUCER NEEDLE?

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 LIGHT SABER INTRODUCER NEEDLE?

The FDA product code for LIGHT SABER INTRODUCER NEEDLE is MDM.

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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 310002K062231MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001K041852MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002K041846SABRESOURCE DRAPE

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Related Devices (Code: MDM)

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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK010184CHESS HAND SURGERY SYSTEMCanica Design, 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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