Atlas FDA

DILECTRON URINARY CONDUCTIVITY PROBE

FDA 510(k) clearance K891681 · decided 1990-05-01

Clearance details

K-number
K891681
Device name
DILECTRON URINARY CONDUCTIVITY PROBE
Applicant
Gyrus Medical , Ltd.
Decision
Substantially Equivalent
Date received
1989-03-22
Decision date
1990-05-01
Days to decision
405 days
Clearance type
Traditional
Product code
JRE
Device class
1
Regulation number
862.2800
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
England, GB
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
URINE REAGENTS STRIPS-8 PARAMETERS (MODIFICATION) (K954977)Teco Diagnostics1996-03-11
MODEL 2721 CLINICAL REFRACTOMETER (K941901)Vee Gee Scientific, Inc.1995-01-17
MODEL 2730 CLINICAL REFRACTOMETER (K941906)Vee Gee Scientific, Inc.1995-01-17
MODEL 2740 CLINICAL REFRACTOMETER (K941903)Vee Gee Scientific, Inc.1995-01-17
MODEL 3461 CLINICAL REFRACTOMETER (K941905)Vee Gee Scientific, Inc.1994-12-13
MODEL 3471 CLINICAL REFRACTOMETER (K941902)Vee Gee Scientific, Inc.1994-12-13
MODEL A300CL CLINICAL REFRACTOMETER (K941904)Vee Gee Scientific, Inc.1994-12-13
ATAGO URINE SPECIFIC GRAVITY & SERUM (K842168)Kyoto Diagnostics, Inc.1984-07-16
SPECIFIC GRAVITY INSTRUMENT (K831213)Iris1983-06-30
REAGENT STRIPS FOR URINALYSIS (K811342)Miles Laboratories, Inc.1981-09-01
NIKON URINE REFRACTOMER SG-1 (K802959)Nippon Kogaku, Inc.1980-12-19
BIOVATION DIGITAL URINOMETER (K790862)Biovation, Inc.1979-06-28

Recalls involving this device

No recalls on record reference this clearance.