Titan Gel High Resolution Serum Protein
FDA 510(k) K821688 · Helena Laboratories
510(k) numberK821688
Submission
- Device name
- Titan Gel High Resolution Serum Protein
- Applicant
- Helena Laboratories
Mchenry, IL, US - Received
- June 8, 1982
- Decision date
- June 22, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JJN – Apparatus, Electrophoresis, For Clinical Use
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.2485
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JJN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K924021 | Power SupplyJJN · Traditional | The Binding Site, Ltd. | 01/28/1993SE |
| K924020 | Electrophoresis TankJJN · Traditional | The Binding Site, Ltd. | 12/28/1992SE |
| K882344 | Electr-TransblotterJJN · Traditional | The W.E.P. Co. | 01/13/1989SE |
| K881852 | Rep SP Electrophoresis System Cat No. 3170JJN · Traditional | Helena Laboratories | 07/08/1988SE |
| K882163 | Helena Rep Gel ProcessorJJN · Traditional | Helena Laboratories | 06/20/1988SE |
| K873352 | Rapid Electrophoresis System (Rep)JJN · Traditional | Helena Laboratories | 09/08/1987SE |
| K864436 | Stavip 3000JJN · Traditional | Roseburg SA | 03/16/1987SE |
| K861414 | Electrophoresis Work Center (Ewc)JJN · Traditional | Helena Laboratories | 08/26/1986SE |
| K841407 | Isogel AgaroseJJN · Traditional | Fmc Corp. | 07/16/1985SE |
| K844710 | Eurochima Serum Protein Electrophoresis MethodJJN · Traditional | Logos Scientific, Inc. | 01/07/1985SE |
More from Logos Scientific, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K213396 | SPIFE A1AT kitOBZ · Traditional | 10/13/2022SE |
| K192931 | V8 Nexus Hemoglobin Ultrascreen, V8 AFSA2 Hemo ControlGKA · Traditional | 04/19/2022SE |
| K131479 | V8 SP Normal Control, Abnormal ControlJJY · Traditional | 10/07/2013SE |
| K100103 | Specialty Assayed CONTROL-2GGC · Traditional | 12/15/2010SE |
| K061991 | Plateletworks Arachidonic Acid, Model Pw-AcaGHR · Traditional | 02/23/2007SE |
| K061069 | Spife IFE-15 Pentavalent, Model 3456, Spife IFE-9 Pentavalent Kit, Model 3457, Spift…CFF · Traditional | 07/06/2006SE |
| K061014 | Actalyke QC Kit, Models Aqc-Hp and Aqc-LpJPA · Special | 05/10/2006SE |
| K050053 | Hemoram/Aggram AnalyzerJPA · Traditional | 07/11/2005SE |
| K024162 | Spife 3000 Titan Gel Igg Ief Kit, Model 3389CFF · Traditional | 02/19/2003SE |
| K023761 | Plateletworks, Models Pw-A, Pw-CJOZ · Traditional | 02/14/2003SE |
Questions and answers
When was Titan Gel High Resolution Serum Protein cleared by the FDA?
Titan Gel High Resolution Serum Protein (K821688) received a 510(k) decision of Substantially Equivalent on June 22, 1982, 14 days after the submission was received.
What is the product code of K821688?
The FDA product code is JJN – Apparatus, Electrophoresis, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2485.