FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MAGNET PAD

K Number: K896802 · Decision Dec 27, 1989
Classifications
1
FEI Numbers
303
Registration Numbers
304
Same Product Code
2
Applicant Total
28
Review Days
26

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Basic Information

Device Name
MAGNET PAD
K Number
K896802
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Westmark, Sterile Packing Systems, Inc. (Sps)
Date Received
December 1, 1989
Decision Date
December 27, 1989
Product Code
LXG
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LXG), ordered by most recent decision date.

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Other Clearances by Westmark, Sterile Packing Systems, Inc. (Sps)

K Number Device Name
K896800 IRRIGATION TRAY
K896799 PARACERVICAL/PUDENDAL TRAYS
K896559 INFANT FEEDING TUBE
K896794 SPECIMEN CONTAINER
K896806 CATHETER PLUG/PROTECTOR
K896798 TRACHEOSTOMY TRAY
K896797 SUCTION CATHETER KIT
K896215 MERCY HIP/KNEE PACK
K896804 MANIFOLD
K896556 UNIVERSAL POOLE SUCTION TUBE
Search all 28 clearances from Westmark, Sterile Packing Systems, Inc. (Sps) →