Data / Medical devices / United States / Medical Chemical Corporation
Medical Chemical Corporation: FDA-registered device maker in Torrance, CA, United States, 10 510(k) clearances
Medical Chemical Corporation is registered with the FDA (registration 2013736) in Torrance, CA, United States. It lists 79 device types. The FDA files 10 510(k) clearances under its listings, the newest dated May 29, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2013736
- Address
- 19430 Van Ness Ave, Torrance, CA, United States, 90501
- Owner or operator
- MEDICAL CHEMICAL CORPORATION (2013736)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- December 9, 1977
- Registered through
- 2026
- Brand names listed
- "A", 0.1%, 02%, 025%, 1%, 5%, ACETIC ACID, ACETIC ACID 1% and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 29, 2015 | K150887 | Para-Fix C&S Medium | JSM | Substantially Equivalent | Medical Chemical Corporation | accessdata.fda.gov |
| February 25, 2015 | K141506 | MCC Para-Fix CARY BLAIR MEDIUM | JSM | Substantially Equivalent | Medical Chemical Corporation | accessdata.fda.gov |
| May 27, 2004 | K032897 | C. DIFFICILE TOXIN A + B FECAL ANTIGEN DETECTION MICROWELL ELISA KIT MODEL; CDIFF-96 | LLH | Substantially Equivalent | Ivd Research, Inc. | accessdata.fda.gov |
| July 10, 2003 | K031059 | IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96 | MHJ | Substantially Equivalent | Ivd Research, Inc. | accessdata.fda.gov |
| March 5, 2003 | K024113 | IVD CRYPTO/GIARDIA DFA | MHI | Substantially Equivalent | Ivd Research, Inc. | accessdata.fda.gov |
| September 17, 2002 | K020583 | IVD GIARDIA ANTIGEN DETECTION ASSAY MODEL GL-96 | MHI | Substantially Equivalent | Ivd Research, Inc. | accessdata.fda.gov |
| January 22, 2001 | K002011 | GLUTARTEST 1 REAGENT STRIP | MSY | Substantially Equivalent | Integrated Biomedical Technology, Inc. | accessdata.fda.gov |
| August 10, 1995 | K914749 | WAVICIDE(R) -01 | MED | Substantially Equivalent | Wave Energy Systems, Inc. | accessdata.fda.gov |
| May 9, 1994 | K941129 | CON-KIT | LKS | Substantially Equivalent | Medical Chemical Corp. | accessdata.fda.gov |
| November 17, 1993 | K924681 | GLUTARALDEHYDE MONITORS | JOJ | Substantially Equivalent | Pymah Corp. | accessdata.fda.gov |
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Updated May 29, 2015. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.