Perkins Mfg. Co.
Mchenry, IL, US
Perkins Mfg. Co. 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 Perkins Mfg. Co. between 1977 and 1997. The busiest year on record is 1989, with 4. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 1 |
| 1989 | 4 |
| 1990 | 3 |
| 1991 | 1 |
| 1992 | 2 |
| 1993 | 1 |
| 1995 | 1 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K972136 | TV MONITOR (P12/17) | IZI | Substantially Equivalent | |
| K954222 | VIDEO ENHANCEMENT UNIT | LLZ | Substantially Equivalent | |
| K926348 | SC1000 SCAN CONVERTER | LMB | Substantially Equivalent | |
| K920550 | DISPLAY PROCESSOR - MODEL IDP5100 | JAA | Substantially Equivalent | |
| K915232 | GRUNDIG ELECTRONICS VARIOUS MODELS | IZI | Substantially Equivalent | |
| K910384 | VIDEO ANNOTATOR MODEL PK2310 | JAA | Substantially Equivalent | |
| K904986 | PROGRAMMABLE VIDEO CONTROLLER MODEL PK2060 | JAA | Substantially Equivalent | |
| K904540 | VIDEO SYSTEM INTERFACE MODELS | IZI | Substantially Equivalent | |
| K896615 | CINE CAMERA CONTROL MODEL PK2037 | IZJ | Substantially Equivalent | |
| K895500 | PATIENT POSITIONING ACCESSORIES | IYE | Substantially Equivalent | |
| K893644 | PK2025/PK2045 PROGRAMMABLE VIDEO CONTROLLER | JAA | Substantially Equivalent | |
| K892934 | 1 VIDEO TAPE RECORDER MODEL BK-224 H | OXO | Substantially Equivalent | |
| K885126 | PHILIPS RT250 COLLIMATOR (PK8050) | KQA | Substantially Equivalent | |
| K770071 | PINLOCK CONTAINER | KDT | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- IYEAccelerator, Linear, Medical
- IZJCamera, X-Ray, Fluorographic, Cine Or Spot
- KDTContainer, Specimen Mailer And Storage, Sterile
- KQADevice, Beam Limiting, X-Ray, Therapeutic
- LMBDevice, Digital Image Storage, Radiological
- OXOImage-Intensified Fluoroscopic X-Ray System, Mobile
- LLZSystem, Image Processing, Radiological
- IZISystem, X-Ray, Angiographic
- JAASystem, X-Ray, Fluoroscopic, Image-Intensified
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