Superior Healthcare Group, Inc.
Cumberland, RI, US
Superior Healthcare Group, Inc. appears in FDA device records in Cumberland, RI. 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 Superior Healthcare Group, Inc. between 1985 and 1993. The busiest year on record is 1989, with 5. The most recent is 1993, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 1 |
| 1988 | 2 |
| 1989 | 5 |
| 1990 | 3 |
| 1991 | 1 |
| 1993 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K925530 | INSTRUMENT WARMER | FMS | Substantially Equivalent | |
| K924764 | OVERTUBE FOR ENDSCOPIC LIGATOR | MNK | Substantially Equivalent | |
| K905755 | NON-STERILE PATIENT EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K903347 | SODIUM CHLORIDE SOLUTION | FOZ | Substantially Equivalent | |
| K904216 | STERILE WATER SOLUTION CATALOG # 10000 | JOL | Substantially Equivalent | |
| K903340 | STERILE URETHRAL CATHETER PROCEDURE KITS | FCM | Unknown | |
| K896321 | NO. 34100 - 8 FR & NO. 34400 - 14 FR CLOSED TRACH. | BSY | Substantially Equivalent | |
| K894676 | STERILE LATEX EXAM GLOVES | LYY | Substantially Equivalent | |
| K891445 | LATEX EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K892426 | NO. 86500 - ENDOSCOPIC JET WASHER | OCX | Substantially Equivalent | |
| K885339 | FLOW THRU 16,18,20,22 FR REPLACE. GASTRO TUBE KIT | KNT | Substantially Equivalent | |
| K880201 | REPLACEMENT SILICONE GASTROSTOMY TUBE KIT #87600 | KNT | Substantially Equivalent | |
| K880648 | ENDOSCOPIC ELASTIC BAND LIGATOR | FHN | Substantially Equivalent | |
| K853353 | 88000 GASTROSTOMY-JEJUNAL FEEDING TUBE KIT | KNT | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- FMSBed, Pediatric Open Hospital
- JOLCatheter And Tip, Suction
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- BSYCatheters, Suction, Tracheobronchial
- MNKEndoscopic Bite Block
- OCXEndoscopic Irrigation/Suction System
- LYYLatex Patient Examination Glove
- FHNLigator, Hemorrhoidal
- FCMTray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)
- KNTTubes, Gastrointestinal (And Accessories)
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
