The following data is part of a premarket notification filed by Precision Biologicals, Inc. with the FDA for Cryo Check Abnormal Reference Check I & Ii.
| Device ID | K952624 |
| 510k Number | K952624 |
| Device Name: | CRYO CHECK ABNORMAL REFERENCE CHECK I & II |
| Classification | Control, Plasma, Abnormal |
| Applicant | PRECISION BIOLOGICALS, INC. 900 WINDMILL ROAD UNIT 100 Dartmouth, Nova Scotia, CA B3b 1p7 |
| Contact | Stephen L Duff |
| Correspondent | Stephen L Duff PRECISION BIOLOGICALS, INC. 900 WINDMILL ROAD UNIT 100 Dartmouth, Nova Scotia, CA B3b 1p7 |
| Product Code | GGC |
| CFR Regulation Number | 864.5425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-06-08 |
| Decision Date | 1995-10-30 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00843876000091 | K952624 | 000 |
| 00843876000084 | K952624 | 000 |
| 00843876000077 | K952624 | 000 |