510(k) K872688
- Device
- IAFP MUELLER HINTON AGAR W/5% SHEEP BLOOD
- Applicant
- I.A.F. PRODUCTION, INC.
- 510(k) number
- K872688
- Product code
- LKA
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1987-08-11
- Date received
- 1987-07-07
- Regulation
- 866.1700
- Classification name
- Culture Media, Antimicrobial Susceptibility Test
- Medical specialty
- Microbiology
- Review panel
- Microbiology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- FRANCOIS MORIN
- Address
- 527, Boul. Des Prairies Laval, Que. H7n-423 CA
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code LKA #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K872686 | IAFP MUELLER HINTON AGAR | I.A.F. Production, Inc. | 1987-08-11 |
| K872687 | IAFP MUELLER HINTON AGAR W/HEMO. W/CVA ENRICHMENT | I.A.F. Production, Inc. | 1987-08-11 |
| K833207 | AK AGAR 2 | Acumedia Manufacturers, Inc. | 1983-10-27 |
| K833218 | YEAST BEEF AGAR-ANTIBIOTIC MED.4 | Acumedia Manufacturers, Inc. | 1983-10-27 |
Legacy Summary#
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FDA Review#
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