Atlas FDA

WILLIAMS MEDIUM E POWDER

FDA 510(k) clearance K861885 · decided 1986-05-29

Clearance details

K-number
K861885
Device name
WILLIAMS MEDIUM E POWDER
Applicant
Hazleton Research Products, Inc.
Decision
Substantially Equivalent
Date received
1986-05-16
Decision date
1986-05-29
Days to decision
13 days
Clearance type
Traditional
Product code
KIT
Device class
1
Regulation number
864.2220
Medical specialty
Hematology
Advisory committee
Hematology
Location
Denver, PA, 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
AMNIO-GROW TM (K892938)Inovar Biologicals, Inc.1989-05-22
ENDOTHELIAL GROWTH MEDIUM (EGM) (K890701)Clonetics Corp.1989-02-24
MELANOCYTE GROWTH MEDIUM (MGM) (K890700)Clonetics Corp.1989-02-24
ABC, ABC-1X, ABC(TM) (K890482)Cell Ent., Inc.1989-02-10
ALPHACALF SERUM (K884654)Hyclone Laboratories, Inc.1988-11-30
HBSS W/O CALC CHLOR/MAG SULF/PHEN RED/SB NO. H4891 (K884573)Sigma Chemical Co.1988-11-22
RPMI-1640 HYBRI-MAX, PROD. NO. R5382 (K884572)Sigma Chemical Co.1988-11-22
DME & HAM'S NUTRIENT MIXTURE, PROD. NO. D9785 (K884574)Sigma Chemical Co.1988-11-22
ALLOPREP SYSTEM (K883065)Osteotech, Inc.1988-10-13
FBS, EQ., OR FETAL BOVINE SERUM EQUIVALENT (K884031)Regency Biotech1988-10-06
MEDIUM 199 W/EBSS (CATALOG NO. 200-2037) (K883951)J R Scientific1988-09-30
CHANG MEDIUM (ADDITIONAL INDICATIONS) (K883682)Hana Biologics, Inc.1988-09-16

Recalls involving this device

No recalls on record reference this clearance.