Ampco Procedure Trays / Packs

FDA 510(k) K843114 · Associated Medical Products Co.

Unknown

510(k) numberK843114

Submission

Device name
Ampco Procedure Trays / Packs
Applicant
Associated Medical Products Co.
Walker, MI, US
Received
August 8, 1984
Decision date
August 8, 1984
Decision
Unknown (SESP)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Associated Medical Products Co.

510(k)DeviceDecision
K932221Neurological or Crani Trays (Packs)LRO · Traditional 03/19/1997SE
K932216C-Section, Labor & Delivery Trays (Packs)MLS · Traditional 04/19/1994SESK
K930507Custom Orthopaedic Trays (Packs)HTS · Traditional 02/22/1994SE
K932217Major, Minor, Basin Trays (Packs)LRO · Traditional 11/15/1993SESK
K932220Lap Choly Trays (Packs)LRO · Traditional 09/27/1993SESK
K932218Cardiac Cath or Angiographic TraysDQO · Traditional 08/27/1993SEKD
K932219Suture Set or Laceration Trays (Packs)KDD · Traditional 07/09/1993SESK
K842983Ampco Opthalmic TrayHOZ · Traditional 05/22/1985SE
K823839Ampco Kidney Dialysis TrayKOC · Traditional 03/29/1983SE
K821579Skin Scrub-TrayLDR · Traditional 07/21/1982SE

Questions and answers

When was Ampco Procedure Trays / Packs cleared by the FDA?

Ampco Procedure Trays / Packs (K843114) received a 510(k) decision of Unknown on August 8, 1984, 0 days after the submission was received.