Nellcor, Inc.
Mchenry, IL, US
Nellcor, Inc. appears in FDA device records in Mchenry, IL. FDA records list 18 510(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
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Nellcor, Inc. between 1982 and 1995. The busiest year on record is 1995, with 5. The most recent is 1995, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 1 |
| 1984 | 1 |
| 1986 | 2 |
| 1988 | 1 |
| 1990 | 3 |
| 1991 | 1 |
| 1993 | 2 |
| 1994 | 2 |
| 1995 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K953472 | NELLCOR SYMPHONY N-3100 BLOOD PRESSURE MONITOR | DXN | Substantially Equivalent | |
| K952316 | NELLCOR SYMPHONY N-3000 PULSE OXIMETER | DQA | Substantially Equivalent | |
| K952222 | NELLCOR N-20PA PORTABLE PULSE OXIMETER | DQA | Substantially Equivalent | |
| K942347 | NELLCOR SYMPHONY PULSE OXIMETER MODEL N-3000 | DQA | Substantially Equivalent | |
| K945947 | NELLCOR SYMPHONY(TM) N-3100 BLOOD PRESSURE MONITOR AND CONNECTED TO THE NELLCOR SYMPHONY(TM) N-3000 PULSE OXIMETER | DXN | Substantially Equivalent | |
| K944760 | DURA-Y OXYGEN TRANSDUCER, EAR CLIP | DPZ | Substantially Equivalent | |
| K944400 | PEDI-CAP | CCK | Substantially Equivalent | |
| K915494 | NELLCOR STAT-CAP AIRWAY CO2 INDICATOR, MODEL N-60 | CCK | Substantially Equivalent | |
| K915699 | NELLCOR PORTABLE PULSE OXIMETER MODEL N-20 | DQA | Substantially Equivalent | |
| K913695 | NELLCOR(R) N-180 PULSE OXIMETER | DQA | Substantially Equivalent | |
| K904039 | REFLECTANCE SENSOR (RS-10) | DQA | Substantially Equivalent | |
| K901399 | POWERBASE II (PB2) | DQA | Substantially Equivalent | |
| K896629 | NELLCOR MODEL N-2500 ANESTHESIA SAFETY MONITOR | CBS | Substantially Equivalent | |
| K884142 | OXINET N-7500 PULSE OXIMETRY NETWORK | DXH | Substantially Equivalent | |
| K862812 | NELLCOR MVP, MODEL N-1000 | DQA | Substantially Equivalent | |
| K863784 | NELLCOR N-200 (PULSE OXIMETER) | DQA | Substantially Equivalent | |
| K844256 | NELLCOR PULSE OXIMETER N-10 | DQA | Substantially Equivalent | |
| K822909 | PULSE OXIMETER MODEL 100 | DQA | 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.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Nellcor, Inc. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Nellcor, Inc.. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain