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FDA 510(k)

MEGA LUMBAR PUNCTURE KIT

K-Number: K910089 · 1991-06-20

ApplicantMegadyne Medical Products, Inc.
Decision Date1991-06-20
Product CodeFMJ
Advisory CommitteeHO
DecisionUnknown

Device Summary

MEGA LUMBAR PUNCTURE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Megadyne Medical Products, Inc.. It received FDA 510(k) clearance on 1991-06-20 under 510(k) number K910089. The device is classified under product code FMJ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEGA LUMBAR PUNCTURE KIT?

MEGA LUMBAR PUNCTURE KIT is a medical device that received FDA 510(k) clearance on 1991-06-20. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K910089.

When did MEGA LUMBAR PUNCTURE KIT receive FDA 510(k) clearance?

MEGA LUMBAR PUNCTURE KIT received FDA 510(k) clearance on 1991-06-20, under 510(k) number K910089.

Who is the listed applicant for MEGA LUMBAR PUNCTURE KIT?

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

What is the FDA product code for MEGA LUMBAR PUNCTURE KIT?

The FDA product code for MEGA LUMBAR PUNCTURE KIT is FMJ.

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Other records listing Megadyne Medical Products, 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.

K233644Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)K213696ETHICON Megadyne Electrosurgical GeneratorK200250Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF SensorK193145Ethicon Megadyne Electrosurgical Generator, Bipolar FootswitchK191328Megadyne Foot SwitchK080741MEGA SOFT REUSABLE PATIENT RETURN ELECTRODE

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Related Devices (Code: FMJ)

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.

K170305Spinal Manometer NRFit; Spinal Manometer LUERPAJUNK GmbH MedizintechnologieK032432BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETERBusse Hospital Disposables, Inc.K970287LUMBAR PUNCTURE KITB.Braun Medical, Inc.K963570SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)Smiths Industries Medical Systems, Inc.K882405HYPODERMIC NEEDLE SHEATH HOLDERAnsr Ent., 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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