JMS Halo Application Tray

FDA 510(k) K864969 · Jerome Medical

Unknown

510(k) numberK864969

Submission

Device name
JMS Halo Application Tray
Applicant
Jerome Medical
Mt Laurel, NJ, US
Received
December 22, 1986
Decision date
February 18, 1987
Decision
Unknown (SESD)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KDD – Kit, Surgical Instrument, Disposable
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

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K936255Custom CV PackKDD · Traditional Associated Medical03/31/1994SN
K932219Suture Set or Laceration Trays (Packs)KDD · Traditional Associated Medical Products Co.07/09/1993SESK
K923176Surgical Instrument Kit, DisposableKDD · Traditional Ulti-Med Intl., Inc.06/17/1993SE
K925905Kit, Surgical Instrument, DisposableKDD · Traditional Kay Medical Concepts06/16/1993SESK
K924958Biopsy/Myelo/Arthro/Amniocent/Basic Skin Prep TrayKDD · Traditional Medical Insights, Inc.06/07/1993SEKD
K925215Sterile Surgical Instrument TraysKDD · Traditional American Healthcare Supply Co., Inc.06/01/1993SEKD

More from American Healthcare Supply Co., Inc.

510(k)DeviceDecision
K051918Resolve Open Back Halo RingsHAX · Special 08/17/2005SE
K930021J TongsHAX · Traditional 12/06/1995SE
K930153System III Halo RingJEC · Traditional 08/06/1993SE
K882877JMS Cervical Traction Device/Halo DeviceJEC · Traditional 09/30/1988SE
K870053Torquedriver WrenchHXC · Traditional 03/11/1987SE
K844490Traction AccessoriesILZ · Traditional 02/21/1985SE
K822780Cervical BraceJEC · Traditional 10/06/1982SE
K821582Warm'N Form Sports SupportsIQI · Traditional 06/10/1982SE

Questions and answers

When was JMS Halo Application Tray cleared by the FDA?

JMS Halo Application Tray (K864969) received a 510(k) decision of Unknown on February 18, 1987, 58 days after the submission was received.

What is the product code of K864969?

The FDA product code is KDD – Kit, Surgical Instrument, Disposable, a Class I (low risk) device regulated under 21 CFR 878.4800.