510(k) K820437
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