Tillotson Healthcare Corp.
Bedford, NH, US
Tillotson Healthcare Corp. appears in FDA device records in Bedford, NH. FDA records list 20 510(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
- 20
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 20 510(k) clearances for Tillotson Healthcare Corp. between 1995 and 2002. The busiest year on record is 2001, with 7. The most recent is 2002, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1995 | 3 |
| 1996 | 2 |
| 1997 | 2 |
| 1998 | 1 |
| 1999 | 2 |
| 2000 | 2 |
| 2001 | 7 |
| 2002 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K021007 | ULTRA PRESERVE WITH ALOE VERA (GREEN) NATURAL RUBBER LATEX EXAMINATION GLOVE MADE FROM ALLOTEX AN ENZYME TREATED NATURAL | LYY | Substantially Equivalent | |
| K013324 | HPI SENSI GRIP STERILE POWDERED LATEX SURGICAL GLOVE,WITH LABELED PROTEIN CONTENT AND MADE FROM ALLOTEX AN ENZYME TREAT | KGO | Substantially Equivalent | |
| K013016 | TRUE ADVANTAGE NON-STERILE POWDER FREE PURPLE NITRILE EXAMINATION GLOVE | LZA | Substantially Equivalent | |
| K013286 | CYMUNVERA POWDER FREE GREEN NATURAL RUBBER LATEX PATIENT EXAMINATION GLOVE LINED WITH ALOE VERA | LYY | Substantially Equivalent | |
| K011497 | CYMUN-NBR POWDER FREE BLUE NITRILE EXAMINATION GLOVE | LZA | Substantially Equivalent | |
| K002718 | ULTRA CARE 2 LATEX EXAMINATION GLOVES MADE FROM ALLOTEX (ENZYME TREATED) NATURAL RUBBER LATEX WITH A PROTEIN CONTENT LAB | LYY | Substantially Equivalent | |
| K004048 | SENSIGRIP LTC POWDER FREE LATEX EXAMINATION GLOVE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS) | LYY | Substantially Equivalent | |
| K002719 | FORMULA ONE POWDERED LATEX EXAMINATION GLOVE, WITH PROTEIN CONTENT LABELING CLAIM 200 MICROGRAMS OR LESS AND MADE FROM A | LYY | Substantially Equivalent | |
| K002720 | FORMULA ONE STERILE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS) MADE FROM ALLO | LYY | Substantially Equivalent | |
| K000745 | SENSI GRIP LATEX EXAMINATION GLOVE, POWDERED CONTAINS 200 MCGM OR LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER GRAM | LYY | Substantially Equivalent | |
| K992428 | ACCUTOUCH POWDER FREE NATURAL RUBBER LATEX PATIENT EXAMINATION GLOVE | LYY | Substantially Equivalent | |
| K982505 | ULTRA CARE NON-STERILE POWDER FREE (GREEN) NATURAL RUBBER LATEX PATIENT EXAMINATION GLOVE | LYY | Substantially Equivalent | |
| K974065 | POWDER FREE HYPROALLERGENIC EXAMINATION GLOVE (WITH LOW PROTEIN CLAIM) | LYY | Substantially Equivalent | |
| K972009 | PURE ADVANTAGE NITRILE HYPOALLERGENIC SURGICAL GLOVE | KGO | Substantially Equivalent | |
| K971945 | PURE ADVANTAGE POWDER FREE NITRILE HYPOALLERGENIC SURGICAL GLOVE | KGO | Substantially Equivalent | |
| K960247 | ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE | LYY | Substantially Equivalent | |
| K960225 | POWDER FREE PLUS HYPOALLERGENIC (WITH LABELED PROTEIN CONTENT) PATIENT EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K954855 | POWDER FREE PLUS PATIENT EXAMINATION GLOVE | LYY | Substantially Equivalent | |
| K954574 | PURE ADVANTAGE NITRILE HYPOALLERGENIC PATIENT EXAMINATION GLOVES | LZA | Substantially Equivalent | |
| K954573 | PURE ADVANTAGE POWDER FREE NITRILE HYPOALLERGENIC PATIENT EXAMINATION GLOVES | LZA | 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
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Data as of , FDA export datePage updated Source: openFDA, public domain