Atlas FDA

VERSABLOT

FDA 510(k) clearance K884258 · decided 1988-12-14

Clearance details

K-number
K884258
Device name
VERSABLOT
Applicant
American Bionetics, Inc.
Decision
Substantially Equivalent
Date received
1988-10-11
Decision date
1988-12-14
Days to decision
64 days
Clearance type
Traditional
Product code
KPA
Device class
1
Regulation number
864.3800
Medical specialty
Pathology
Advisory committee
Pathology
Location
Hayward, CA, 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
PROFIBLOT (K933996)Tecan U.S., Ltd.1994-01-28
WESCOR MODEL 7300 AEROSPRAY GRAM STAINER (K881592)Wescor, Inc.1988-05-13
LX-100 SLIDE STAINER (K880745)Innovative Medical Systems, Inc.1988-04-27
WESBLOT PROCESSOR (K874887)American Bionetics, Inc.1988-03-24
SAKURA DRS-60 AUTOMATIC SLIDE STAINER (K874897)Sakura Finetek U.S.A., Inc.1988-01-05
HISTOMATIC SLIDE STAINER, CODE-ON VERSION (K872916)Fisher Scientific Co., LLC1987-09-14
MST-1050-II X-RAY UNIT (K853210)Radiological Engineering, Inc.1985-10-10
CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERS (K850157)Shaban Mfg. Co.1985-02-27
PUMP TUBE SETS FOR HEMA-TEK I & II SLIDE STAINERS (K850333)Shaban Mfg. Co.1985-02-27
MIDAS II AUTOMATIC STAINER (K842077)Innovative Medical Systems, Inc.1984-07-27
WESCOR 7100 AEROSPRAY SLIDE STAINER (K833295)Wescor, Inc.1983-10-31
MIDAS 6000 AUTOMATIC STAINER (K832994)Innovative Medical Systems, Inc.1983-09-29

Recalls involving this device

No recalls on record reference this clearance.