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FDA 510(k)

LIGHT SABER SPINAL NEEDLE

K-Number: K021084 · 2002-07-03

ApplicantMinrad, Inc.
Decision Date2002-07-03
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIGHT SABER SPINAL 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 2002-07-03 under 510(k) number K021084. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT SABER SPINAL NEEDLE?

LIGHT SABER SPINAL NEEDLE is a medical device that received FDA 510(k) clearance on 2002-07-03. The listed applicant is Minrad, Inc.. The 510(k) number is K021084.

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

LIGHT SABER SPINAL NEEDLE received FDA 510(k) clearance on 2002-07-03, under 510(k) number K021084.

Who is the listed applicant for LIGHT SABER SPINAL 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 SPINAL NEEDLE?

The FDA product code for LIGHT SABER SPINAL NEEDLE is FMF.

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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: FMF)

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.

K262581GraftGun Universal Graft Delivery System (GDS®)SurGenTec, LLCK252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLCK253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., Ltd.

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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