510(k) K831797

HEMOSTATS by I M, Inc. — Product Code HRQ

K831797 is an FDA 510(k) premarket notification submitted by I M, Inc. for the device "HEMOSTATS". The FDA issued a decision of Substantially Equivalent on July 19, 1983. The device falls under product code HRQ (Hemostat), a Class I device regulated under 21 CFR 878.4800. I M, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 19, 1983
Date Received
June 3, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hemostat
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type