The following data is part of a premarket notification filed by American Sterilizer Co. with the FDA for Spordex Culture Media.
Device ID | K850143 |
510k Number | K850143 |
Device Name: | SPORDEX CULTURE MEDIA |
Classification | Culture Media, General Nutrient Broth |
Applicant | AMERICAN STERILIZER CO. 2424 WEST 23RD ST. P.O. BOX 620 Erie, PA 16514 |
Contact | James A Spallina |
Correspondent | James A Spallina AMERICAN STERILIZER CO. 2424 WEST 23RD ST. P.O. BOX 620 Erie, PA 16514 |
Product Code | JSC |
CFR Regulation Number | 866.2350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-01-14 |
Decision Date | 1985-03-05 |