Medical Device Manufacturer · US , Mchenry , IL

Dryden Corp. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1976

Total

Cleared

Denied

Dryden Corp. has 21 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1976 to 1988.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Dryden Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dryden Corp.

21 devices

1-12 of 21

Cleared Sep 06, 1988

PATIENT VENTILATOR ISOLATOR

K880923 · CBK

Anesthesiology · 186d

Cleared Aug 24, 1988

BREATHING CIRCUIT W/HEATED WIRE

K880769 · BZE

Anesthesiology · 177d

Cleared Aug 16, 1988

NONREBREATHING CIRCUIT

General & Plastic Surgery · 28d

Cleared Oct 20, 1987

REUSEABLE BREATHING TUBES

Anesthesiology · 153d

BADGWELL SAMPLING CATHETER

K870858 · CCK

Anesthesiology · 72d

Cleared May 02, 1986

DISPOSABLE BERMAN AND GUEDEL AIRWAYS

K861540 · CAE

Anesthesiology · 8d

Cleared Mar 21, 1985

NASOPHARYNGEAL AIRWAY-ROBERTAZZI

K850644 · BTQ

Anesthesiology · 30d

Cleared Jul 27, 1984

DRYDEN SCAVENGER INTERFACE SYSTEM

K842843

Cardiovascular · 7d

Cleared Jul 06, 1984

DRYDEN INFLATABLE MASK

K842472 · BSJ

Anesthesiology · 11d

Dryden Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Dryden Corp.

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