510(k) K842726
- Device
- DECALCIFIER SOLUTION
- Applicant
- E K IND., INC.
- 510(k) number
- K842726
- Product code
- KDX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-08-03
- Date received
- 1984-07-13
- Regulation
- 864.4010
- Classification name
- Solution, Decalcifier, Acid Containing
- Medical specialty
- Pathology
- Review panel
- Pathology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3004594181
- 9610140
- 1625587
- 3009963993
- 2244900
- 3006365273
- 1045125
- 1419341
- 3008174888
- 1640981
- 2247035
- 2013736
- 1419699
- 1125908
- 2028411
- 3017970519
- 1831638
- 3010194621
- 3007496191
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code KDX #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K872625 | DECALCIFYING SOLUTION | Stephens Scientific | 1987-08-06 |
| K850636 | SIMUTANEOUS FIXATION & DECALCIFYING SOLUTION CAL-E | Fisher Scientific Co., LLC | 1985-03-20 |
| K841488 | DECALCIFIER I | Surgipath Medical Industries, Inc. | 1984-05-02 |
| K822036 | VOLU-SOL DECALCIFER | Volu Sol Medical Industries | 1982-08-03 |
| K821443 | FORMICAL | Lerner Laboratories, Inc. | 1982-06-02 |
| K811801 | CAL-RITE | Richard-Allan Medical Ind., Inc. | 1981-07-28 |
| K810836 | DECALCIFIER II | Surgipath | 1981-04-23 |
Legacy Summary#
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FDA Review#
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