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

PARA-PAK

K Number: K811722 · Decision Jul 15, 1981
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
5
Applicant Total
92
Review Days
27

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Basic Information

Device Name
PARA-PAK
K Number
K811722
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.1850
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Meridian Diagnostics, Inc.
Date Received
June 18, 1981
Decision Date
July 15, 1981
Product Code
HYI
Advisory Committee
Hematology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
HYI Iodine, Grams

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Other Clearances by Meridian Diagnostics, Inc.

K Number Device Name
K993914 PREMIER TOXINS A&B, MODEL 616096
K990263 IMMUNOCARD STAT! E. COLI O157:H7
K984346 PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TEST
K984343 PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST
K983255 MODIFICATION TO: PREMIER PLATINUM HPSA
K982764 PREMIER CRYPTOSPORIDIUM
K982711 PREMIER GIARDIA
K980076 PREMIER PLATINUM HPSA
K980077 PARA-PAK SPINCON
K971585 IMMUNOCARD STAT! ROTAVIRUS
Search all 92 clearances from Meridian Diagnostics, Inc. →