Atlas FDA

LARYNGEAL

FDA 510(k) clearance K853726 · decided 1986-03-12

Clearance details

K-number
K853726
Device name
LARYNGEAL
Applicant
Hood Laboratories
Decision
Substantially Equivalent
Date received
1985-09-06
Decision date
1986-03-12
Days to decision
187 days
Clearance type
Traditional
Product code
FWN
Device class
2
Regulation number
874.3620
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Pembroke, MA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
RUTTER SUPRA STOMAL STENTS (K091135)Boston Medical Products, Inc.2009-09-14
ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1 (K000154)E. Benson Hood Lab, Inc.2000-03-29
MONTGOMERY RADIOPAQUE LARYNGEAL KEEL (K962693)Boston Medical Products, Inc.1996-08-09
LORENZ STENT (K896667)Walter Lorenz Surgical, Inc.1990-02-22
SILICONE LARYNGEAL STENT (K884810)Hood Laboratories1989-05-10
'EXMOOR' DAS GUPTA LARYNGEAL KEEL (K864936)Exmoor Plastics , Ltd.1987-04-27
MONTG. LARYNGEAL KEEL (K842800)Boston Medical Products, Inc.1984-08-02
MONTGOMERY LARYNGEAL STENT (K842287)Boston Medical Products, Inc.1984-06-27
LARYNGEAL STENT (K841347)E. Benson Hood Laboratories, Inc.1984-05-02

Recalls involving this device

No recalls on record reference this clearance.