The following data is part of a premarket notification filed by Healthdyne Cardiovascular, Inc. with the FDA for Isoflo(tm) Amniocentesis Tray.
Device ID | K901643 |
510k Number | K901643 |
Device Name: | ISOFLO(TM) AMNIOCENTESIS TRAY |
Classification | Sampler, Amniotic Fluid (amniocentesis Tray) |
Applicant | HEALTHDYNE CARDIOVASCULAR, INC. 45 PARKER ST., SUITE A Irvine, CA 92618 -1658 |
Contact | Bill Welch |
Correspondent | Bill Welch HEALTHDYNE CARDIOVASCULAR, INC. 45 PARKER ST., SUITE A Irvine, CA 92618 -1658 |
Product Code | HIO |
CFR Regulation Number | 884.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-04-09 |
Decision Date | 1990-07-25 |