Carr-Scarborough Microbiologicals, Inc.
Mchenry, IL, US
Carr-Scarborough Microbiologicals, Inc. appears in FDA device records in Mchenry, IL. FDA records list 24 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for Carr-Scarborough Microbiologicals, Inc. between 1979 and 1994. The busiest year on record is 1981, with 6. The most recent is 1994, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1980 | 1 |
| 1981 | 6 |
| 1982 | 6 |
| 1986 | 3 |
| 1989 | 3 |
| 1991 | 2 |
| 1994 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K944554 | BRAIN HEART INFUSION AGAR | JSO | Substantially Equivalent | |
| K941985 | MUELLER HINTON AGAR W/OXACILLIN | JTZ | Substantially Equivalent | |
| K905472 | LAP DISCS | JTO | Substantially Equivalent | |
| K905666 | M. CAT. BUTYRATE DISC | JTO | Substantially Equivalent | |
| K891476 | C. ALBICANS SCREEN | JXC | Substantially Equivalent | |
| K882636 | ALN DISCS | JTO | Substantially Equivalent | |
| K882630 | PRO DISCS | JTO | Substantially Equivalent | |
| K863216 | NEIS NZY | JTO | Substantially Equivalent | |
| K860301 | RAPID GLUTAMIC ACID DECARBOXYLASE (GDC) MICROTUBE | JTO | Substantially Equivalent | |
| K860302 | PYR DISCS | JTO | Substantially Equivalent | |
| K822930 | CSM CHROMOGENIC B-LACTAMASE DISC | JTO | Substantially Equivalent | |
| K822518 | CSM BETA-LACTAMASE DISC | Substantially Equivalent | ||
| K820347 | ACCU-STAPH | LHT | Substantially Equivalent | |
| K820346 | CALI-PIPETTE | LIB | Substantially Equivalent | |
| K820345 | CALI-LOOP | LIB | Substantially Equivalent | |
| K820149 | PYR BROTH | JSF | Substantially Equivalent | |
| K812668 | AFB STAIN SET | JTS | Substantially Equivalent | |
| K812274 | AURAMINE O MYCROBACTERIAL STAIN SET | KJK | Substantially Equivalent | |
| K812212 | ACRIDINE ORANGE STAIN | IDC | Substantially Equivalent | |
| K812048 | IDS RAPIDS NH SYSTEMS | JSX | Substantially Equivalent | |
| K812047 | IDS BETA-LACTAMASE DISC | JTO | Substantially Equivalent | |
| K811422 | STREP-ID PLATE | JSI | Substantially Equivalent | |
| K802566 | BETA LACTAMASE REAGENT DISK | JTO | Substantially Equivalent | |
| K791711 | IMPROVED GRAM STAIN REAGENTS | HYI | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- IDCAcridine Orange
- KJKAuramine O
- JSOCulture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar
- JTZCulture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth
- JSICulture Media, Selective And Differential
- JSFCulture Media, Single Biochemical Test
- LIBDevice, General Purpose, Microbiology, Diagnostic
- JTODiscs, Strips And Reagents, Microorganism Differentiation
- HYIIodine, Grams
- JSXKit, Identification, Neisseria Gonorrhoeae
- JXCKit, Screening, Yeast
- JTSStains, Microbiologic
- LHTStaphylococcus Aureus Somatic Antigens
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Carr-Scarborough Microbiologicals, Inc. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Carr-Scarborough Microbiologicals, Inc.. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain