510(k) K905207

MICRO-AIRE SOFT-ICE, COLD THERAPY COMPRESS by Micro Surgical Instruments Corp. — Product Code IME

K905207 is an FDA 510(k) premarket notification submitted by Micro Surgical Instruments Corp. for the device "MICRO-AIRE SOFT-ICE, COLD THERAPY COMPRESS". The FDA issued a decision of SN on January 22, 1991. The device falls under product code IME (Pack, Hot Or Cold, Reusable), a Class I device regulated under 21 CFR 890.5700. Micro Surgical Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
January 22, 1991
Date Received
November 20, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pack, Hot Or Cold, Reusable
Device Class
Class I
Regulation Number
890.5700
Review Panel
PM
Submission Type