Atlas FDA

HYDRAJUST III UROLOGICAL TABLE

FDA 510(k) clearance K860040 · decided 1986-02-10

Clearance details

K-number
K860040
Device name
HYDRAJUST III UROLOGICAL TABLE
Applicant
Mallinckrodt Group, Inc.
Decision
Substantially Equivalent
Date received
1986-01-06
Decision date
1986-02-10
Days to decision
35 days
Clearance type
Traditional
Product code
KQS
Device class
1
Regulation number
876.4890
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Cincinnati, OH, 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
UROTRACT I (K955019)Dornier Medtech America, Inc.1995-12-06
UROVIEW (K872022)Oec-Diasonics, Inc.1987-07-16
RADIOGRAPHIC - LEG SECTION (K864846)American Sterilizer Co.1986-12-24
AMSCO URO-ENDO MOBILE TABLE (K852127)American Sterilizer Co.1985-08-08
UR 150-UR 150T (K801723)Siemens Corp.1980-08-13
HYDRADJUST II UROLOGICAL TABLE (K791699)Sybron Corp.1979-10-22
TABLE, UROSURGICAL (K760522)Mallinckrodt Group, Inc.1976-12-16

Recalls involving this device

No recalls on record reference this clearance.