Atlas FDA

RHINOMANOMETER

FDA 510(k) clearance K896263 · decided 1990-04-16

Clearance details

K-number
K896263
Device name
RHINOMANOMETER
Applicant
Jedmed Instrument Co.
Decision
Substantially Equivalent
Date received
1989-10-31
Decision date
1990-04-16
Days to decision
167 days
Clearance type
Traditional
Product code
BXQ
Device class
2
Regulation number
868.1800
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
St. Louis, MO, 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
VISIONAIR (K221892)Pacificmd Biotech, LLC2022-10-05
SGS ECCOVISIONTM Pharyngometer, SGS ECCOVISIONTM Rhinometer, SGS ECCOVISIONTM Rhino/Pharyngometer (K170071)Sleep Group Solutions2017-11-09
RHINOSTREAM RHINOMANOMETER MODULE (K022311)Rhino Metrics A/S2002-10-04
ECCOVISION ACOUSTIC DIAGNOSTIC IMAGING ACOUSTIC PHARYNGOMETER (K011329)E. Benson Hood Lab, Inc.2002-07-26
RHINOSCAN MODEL SRE2000/ SRE2100 WITH ACOUSTIC RHINOMETRY MODULE (K000406)Rhino Metrics A/S2000-04-17
A1 ACOUSTIC RHINOMETER (K972140)G.M. Instruments , Ltd.1998-09-30
ACOUSTIC RHINOMETER (K921452)Hood Laboratories1993-07-08
MERCURY RHINOMANOMETER (K902120)Life-Tech Intl., Inc.1990-08-06
RHINOTEST MP (K853024)Intertronic, Inc.1985-09-27
RHINOMANOMETERS NR3, NR4 (K851143)And/Or Corp.1985-05-23
RHINOMANOMETER A440 DIGITAL (K844230)Center Laboratories, Inc.1984-11-27

Recalls involving this device

No recalls on record reference this clearance.