510(k) K862223
- Device
- MICRO THIN* PARAFFIN
- Applicant
- RICHARD-ALLAN MEDICAL IND., INC.
- 510(k) number
- K862223
- Product code
- KEO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1986-06-17
- Date received
- 1986-06-11
- Regulation
- 864.4010
- Classification name
- Formulations, Paraffin, All
- Medical specialty
- Pathology
- Review panel
- Pathology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- JULIE POWELL
- Address
- 8850m89, Box 351 Richland MI US 49083 49083
FDA Registration Numbers#
- 3015505238
- 3042200051
- 3004594181
- 3007480628
- 2939821
- 9610140
- 2518071
- 1419341
- 1640981
- 3019387954
- 2247035
- 3008776165
- 2013736
- 1063851
- 3012494290
- 3013182314
- 2083544
- 3010420046
- 3010692993
- 1831638
- 3010973832
- 1055757
- 3007496191
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code KEO #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K893772 | TISSUE EMBEDDING MEDIUM | Stephens Scientific | 1989-06-22 |
| K862141 | HISTOLOGY PARAFFIN | Erie Scientific Co. | 1986-06-13 |
| K861270 | BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED. | Surgipath Medical Industries, Inc. | 1986-04-11 |
| K842053 | PARAPLAST EXTRA TISSUE EMBEDDING MED. | Sherwood Medical Co. | 1984-06-26 |
| K833071 | TECHNICON PARACUT | Technicon Instruments Corp. | 1983-10-14 |
| K831580 | PARAFFIN INFILTRATION MEDIUM | Surgipath Medical Industries, Inc. | 1983-06-17 |
| K812191 | VASPAR SEALENT | American Scientific Products | 1981-08-31 |
| K810568 | PARAFFIN EMBEDDING MEDIUM | Surgipath Medical Industries, Inc. | 1981-03-17 |
| K803241 | HISTOLOGICAL EMBEDDING MEDIA | Miles Laboratories, Inc. | 1981-01-28 |
| K760602 | SORVALL EMBEDDING MEDIUM | E.I. Dupont DE Nemours & Co., Inc. | 1976-09-21 |
Legacy Summary#
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FDA Review#
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