Mcghan Medical Corp.
Mchenry, IL, US
Mcghan Medical Corp. appears in FDA device records in Mchenry, IL. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Mcghan Medical Corp. between 1978 and 1987. The busiest year on record is 1978, with 5. The most recent is 1987, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 5 |
| 1984 | 1 |
| 1985 | 2 |
| 1986 | 3 |
| 1987 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K873476 | MINI-MOTOR HAND ENGINE & ACCESS. DERMABRASION BURS | GEY | Substantially Equivalent | |
| K873475 | MICRO-TORQUE HAND ENGINE & ACCESS. DERMABRA. BURS | GEY | Substantially Equivalent | |
| K870754 | MCGHAN TISSUE EXPANDER FILL SYSTEM | LCJ | Substantially Equivalent | |
| K864185 | MCGHAN LONGTERM MAMMARY EXPANDER, RTV DESIGN | LCJ | Substantially Equivalent | |
| K864184 | MCGHAN LONGTERM MAMMARY EXPANDER/GEL-SALINE DESIGN | LCJ | Substantially Equivalent | |
| K862203 | MCGHAN MAGNA-SITE(TM) TISSUE EXPANDER | LCJ | Substantially Equivalent | |
| K854794 | MCGHAN INTEGRAL VALVE TISSUE EXPANDER | LCJ | Substantially Equivalent | |
| K853014 | MCGHAN TISSUE EXPANDER FILL KIT | LCJ | Substantially Equivalent | |
| K843704 | MCGHAN TISSUE EXPANDER | LCJ | Substantially Equivalent | |
| K781087 | MEDICAL GRADE SILICONE ELASTOMER TUBING | FPK | Substantially Equivalent | |
| K781700 | IONOTPHORETIC APPLICATOR | KTB | Substantially Equivalent | |
| K781491 | PRO-MOLD, CUSTOM EAR | EWD | Substantially Equivalent | |
| K781356 | IMPLANT, EYE SPHERE | HPZ | Substantially Equivalent | |
| K780956 | OTOLOGICAL VENTILATION TUBES | ETD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
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.
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Data as of , FDA export datePage updated Source: openFDA, public domain
