Medical Device Manufacturer · US , Pembroke , MA

Hood Laboratories - FDA 510(k) Cleared Devices

19 submissions · 18 cleared · Since 1985

Total

Cleared

Denied

Hood Laboratories has 18 FDA 510(k) cleared medical devices. Based in Pembroke, US.

Historical record: 18 cleared submissions from 1985 to 1993.

Browse the FDA 510(k) cleared devices submitted by Hood Laboratories Filter by specialty or product code using the sidebar.

Hood Laboratories 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 - Hood Laboratories

19 devices

1-12 of 19

Cleared Jul 08, 1993

ACOUSTIC RHINOMETER

K921452 · BXQ

Anesthesiology · 469d

Cleared May 15, 1992

HOOD NASAL SEPTAL BUTTON

K920994 · LFB

Ear, Nose, Throat · 74d

Cleared Mar 15, 1991

KRUPIN EYE VALVE WITH DISK

K905703 · KYF

Ophthalmic · 85d

Cleared Jan 14, 1991

ELIACHAR MODIFIED ESOPHAGEAL STENT

K904821 · ESW

Gastroenterology & Urology · 82d

Cleared Mar 16, 1990

GIBSON ENDOLYMPHATIC SHUNT

K897049 · ESZ

Ear, Nose, Throat · 88d

HOOD PEDIATRIC TRACHEOSTOMY TUBE

K893866 · BTO

Anesthesiology · 73d

Cleared May 10, 1989

SILICONE LARYNGEAL STENT

K884810 · FWN

Ear, Nose, Throat · 174d

Cleared Mar 17, 1989

HOOD NASAL SPLINT

K890599 · EPP

Ear, Nose, Throat · 39d

Cleared Jan 24, 1989

KRUPIN EYE VALVE W/SCLERAL BUCKLE

K885125 · KYF

Ophthalmic · 43d

Cleared Jun 28, 1988

HOOD TRACHEAL STOMA BUTTON

K882430 · BTO

Anesthesiology · 14d

Cleared Oct 01, 1987

HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES

K873742 · NWA

General & Plastic Surgery · 15d

Hood Laboratories - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Hood Laboratories

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