510(k) K820437

AVES WRIGHT STAIN by Helena Laboratories — Product Code IAF

K820437 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "AVES WRIGHT STAIN". The FDA issued a decision of Substantially Equivalent on March 26, 1982. The device falls under product code IAF (Wright'S Stain), a Class I device regulated under 21 CFR 864.1850. Helena Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 26, 1982
Date Received
February 17, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Wright'S Stain
Device Class
Class I
Regulation Number
864.1850
Review Panel
PA
Submission Type