510(k) K884784

VIRGO(R) MICROWELL ALT ASSAY by Electro-Nucleonics, Inc. — Product Code CKD

K884784 is an FDA 510(k) premarket notification submitted by Electro-Nucleonics, Inc. for the device "VIRGO(R) MICROWELL ALT ASSAY". The FDA issued a decision of Substantially Equivalent on December 29, 1988. The device falls under product code CKD (Hydrazone Colorimetry, Alt/Sgpt), a Class I device regulated under 21 CFR 862.1030. Electro-Nucleonics, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 29, 1988
Date Received
November 15, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hydrazone Colorimetry, Alt/Sgpt
Device Class
Class I
Regulation Number
862.1030
Review Panel
CH
Submission Type