Dryden Corp.
Mchenry, IL, US
Dryden Corp. appears in FDA device records in Mchenry, IL. FDA records list 21 510(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
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Dryden Corp. between 1976 and 1988. The busiest year on record is 1984, with 7. The most recent is 1988, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1979 | 1 |
| 1980 | 1 |
| 1983 | 1 |
| 1984 | 7 |
| 1985 | 1 |
| 1986 | 1 |
| 1987 | 5 |
| 1988 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K880923 | PATIENT VENTILATOR ISOLATOR | CBK | Substantially Equivalent | |
| K880769 | BREATHING CIRCUIT W/HEATED WIRE | BZE | Substantially Equivalent | |
| K882285 | NONREBREATHING CIRCUIT | BTM | Substantially Equivalent | |
| K873928 | UNIVERSAL TOURNIQUET | GAX | Substantially Equivalent | |
| K873927 | REUSEABLE BREATHING TUBES | BZO | Substantially Equivalent | |
| K870859 | BAG-TAIL BLEED VALVE | CAI | Substantially Equivalent | |
| K871386 | BREATHING CIRCUIT | CAI | Substantially Equivalent | |
| K870858 | BADGWELL SAMPLING CATHETER | CCK | Substantially Equivalent | |
| K861540 | DISPOSABLE BERMAN AND GUEDEL AIRWAYS | CAE | Substantially Equivalent | |
| K850644 | NASOPHARYNGEAL AIRWAY-ROBERTAZZI | BTQ | Substantially Equivalent | |
| K842843 | DRYDEN SCAVENGER INTERFACE SYSTEM | Substantially Equivalent | ||
| K842472 | DRYDEN INFLATABLE MASK | BSJ | Substantially Equivalent | |
| K841455 | REUSEABLE NON-CONDUCTIVE FIXED Y | CAI | Substantially Equivalent | |
| K841722 | MASS SPECTROMETER INTERFACE | BZO | Substantially Equivalent | |
| K840431 | SCRATCH & SNIFF FOR ANESTHESIA | CAI | Substantially Equivalent | |
| K841637 | THREE PORT SENSOR MANIFOLD | BZO | Substantially Equivalent | |
| K840205 | DRYDEN MINI BACTERIA FILTER | CAH | Substantially Equivalent | |
| K833066 | DRYDEN MINI BACTERIA FILTER | CAH | Substantially Equivalent | |
| K800155 | DISPOSAL LITER BREATHING BAG | BTC | Substantially Equivalent | |
| K792097 | DRYDEN BACTERIA FILTER | CAH | Substantially Equivalent | |
| K760371 | VENT-O2-CATH | BSY | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- BTQAirway, Nasopharyngeal
- CAEAirway, Oropharyngeal, Anesthesiology
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- BTCBag, Reservoir
- BSYCatheters, Suction, Tracheobronchial
- CAICircuit, Breathing (W Connector, Adaptor, Y Piece)
- CAHFilter, Bacterial, Breathing-Circuit
- BZEHeater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
- BSJMask, Gas, Anesthetic
- BZOSet, Tubing And Support, Ventilator (W Harness)
- GAXTourniquet, Nonpneumatic
- CBKVentilator, Continuous, Facility Use
- BTMVentilator, Emergency, Manual (Resuscitator)
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
