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FDA 510(k)

SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)

K-Number: K963570 · 1996-10-18

ApplicantSmiths Industries Medical Systems, Inc.
Decision Date1996-10-18
Product CodeFMJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22) is the device name listed in this FDA 510(k) record. The listed applicant is Smiths Industries Medical Systems, Inc.. It received FDA 510(k) clearance on 1996-10-18 under 510(k) number K963570. The device is classified under product code FMJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)?

SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22) is a medical device that received FDA 510(k) clearance on 1996-10-18. The listed applicant is Smiths Industries Medical Systems, Inc.. The 510(k) number is K963570.

When did SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22) receive FDA 510(k) clearance?

SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22) received FDA 510(k) clearance on 1996-10-18, under 510(k) number K963570.

Who is the listed applicant for SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)?

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

What is the FDA product code for SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)?

The FDA product code for SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22) is FMJ.

Related Clinical Trials

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.

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Other records listing Smiths Industries Medical Systems, 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.

K972385FENESTRATED FLEXIBLE D.I.C. TRACHEOSTOMY TUBE CUFFEDK965017REGIONAL ANESTHESIA TRAYSK962175PORTEX ADJUSTABLE FLANGE TRACHEOSTOMY TUBEK962931SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KITK960429PER-FIT PERCUTANEOUS TRACHEOSTOMY KIT W/PORTEX TRACHEOSTMY TUBE & DISP. INNER CANNULAK953485SIMS CPAP SYSTEM

View all 22 devices →

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.K910089MEGA LUMBAR PUNCTURE KITMegadyne Medical Products, 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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