510(k) K981391

PAR-ONE by Remel, Inc. — Product Code LIO

K981391 is an FDA 510(k) premarket notification submitted by Remel, Inc. for the device "PAR-ONE". The FDA issued a decision of Substantially Equivalent on July 14, 1998. The device falls under product code LIO (Device, Specimen Collection), a Class I device regulated under 21 CFR 866.2900. Remel, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 14, 1998
Date Received
April 17, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Specimen Collection
Device Class
Class I
Regulation Number
866.2900
Review Panel
MI
Submission Type