FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DAC-CEL HCG

K Number: K810215 · Decision Apr 17, 1981
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
17
Review Days
80

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Basic Information

Device Name
DAC-CEL HCG
K Number
K810215
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Burroughs Wellcome Co.
Date Received
January 27, 1981
Decision Date
April 17, 1981
Product Code
JHI
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JHI Visual, Pregnancy Hcg, Prescription Use

Similar 510(k) Clearances

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Other Clearances by Burroughs Wellcome Co.

K Number Device Name
K820069 WELLCOGEN GROUP B
K813508 SAC-CEL
K810214 DAC-CEL DIAGNATAL
K810213 DAC-CEL TSH
K810212 DAC-CEL T3 UPTAKE
K791231 DAC-CEL T4
K791232 DAC-CEL T3
K781607 STREP-TEX
K780873 THYMUNE-M
K780874 THYMUNE-T
Search all 17 clearances from Burroughs Wellcome Co. →