510(k) K972819

VIGIL TDM CONTROLS by Beckman Instruments, Inc. — Product Code DIF

K972819 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "VIGIL TDM CONTROLS". The FDA issued a decision of Substantially Equivalent on August 13, 1997. The device falls under product code DIF (Drug Mixture Control Materials), a Class I device regulated under 21 CFR 862.3280. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 13, 1997
Date Received
July 29, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drug Mixture Control Materials
Device Class
Class I
Regulation Number
862.3280
Review Panel
TX
Submission Type