The following data is part of a premarket notification filed by Incstar Corp. with the FDA for Bahia Allergen Disc.
Device ID | K873648 |
510k Number | K873648 |
Device Name: | BAHIA ALLERGEN DISC |
Classification | System, Test, Radioallergosorbent (rast) Immunological |
Applicant | INCSTAR CORP. 1990 INSUSTRIAL BLVD. P.O. BOX 285 Stillwater, MN 55082 -0285 |
Contact | John G Yager |
Correspondent | John G Yager INCSTAR CORP. 1990 INSUSTRIAL BLVD. P.O. BOX 285 Stillwater, MN 55082 -0285 |
Product Code | DHB |
CFR Regulation Number | 866.5750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-09-09 |
Decision Date | 1987-10-08 |