Atlas FDA

PEAK FLOW RATE METER

FDA 510(k) clearance K893827 · decided 1989-08-11

Clearance details

K-number
K893827
Device name
PEAK FLOW RATE METER
Applicant
Laytech Medical Co.
Decision
Substantially Equivalent
Date received
1989-05-24
Decision date
1989-08-11
Days to decision
79 days
Clearance type
Traditional
Product code
FFG
Device class
2
Regulation number
876.1800
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Arlington Heights, IL, 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
SURGITEK (R) UROFLOW SYSTEM (K883274)Medical Engineering Corp.1989-02-08
ERIS URO-DIAGNOSTIC SYSTEM (K850169)Eris Medical Technology1985-04-22
1URO-LOG HOME DIAGNOSTIC PACK (K844338)Epcom Medical Systems, Inc.1985-02-25
URINARY DRAINAGE CONTAINER 2012-WITH (K843441)Vital Metrics, Inc.1985-01-03
URINARY DRAINAGE CONTAINER 2013 WITH (K843442)Vital Metrics, Inc.1985-01-03
ACCUMETER ELECTRONIC URINEMETER SYSTEM (K844030)Travenol Laboratories, S.A.1984-11-20
UROPUMP MODEL 1711 (K843224)Life-Tech Intl., Inc.1984-10-19
UROMETER (K833043)Browne Medical, Inc.1984-02-04
VITAL METRICS URINE MONITORING SYSTEM (K813641)Vital Metrics, Inc.1982-03-01
UREOFIX 500 URINE MEASURING SYSTEM (K813082)Burron Medical Products, Inc.1981-12-31
UROFLOWMETER (K811925)C.R. Bard, Inc.1981-09-08
URITRON URINE METER (K790894)Joseph F. Daniel, C.R.N.A.1979-09-07

Recalls involving this device

No recalls on record reference this clearance.