FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AGAR REDUCTION IN FORMULA FOR PDC 110 & 310 MEDIA

K Number: K863164 · Decision Aug 27, 1986
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
110
Applicant Total
25
Review Days
9

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AGAR REDUCTION IN FORMULA FOR PDC 110 & 310 MEDIA
K Number
K863164
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2390
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Precision Dynamics Corp.
Date Received
August 18, 1986
Decision Date
August 27, 1986
Product Code
JSM
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JSM Culture Media, Non-Propagating Transport

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JSM), ordered by most recent decision date.

View all

Other Clearances by Precision Dynamics Corp.

K Number Device Name
K020718 SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE
K994353 SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565
K994263 SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540
K990737 'ECURLINE UMBILICAL CORD CLAMP #3500
K884357 PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM
K882580 MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE
K874665 SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY
K873369 SECURLINE FRANSEENE NEEDLE
K872507 PRECISION CULTURE C.A.T.S. COLLECT/TRANS HSV I/II
K851364 FRANZEN NEEDLE GUIDE FOR TRANSRECTAL PROSTATE BIOP
Search all 25 clearances from Precision Dynamics Corp. →