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

PINLOCK CONTAINER

K Number: K770071 · Decision Feb 24, 1977
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
11
Applicant Total
14
Review Days
42

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Basic Information

Device Name
PINLOCK CONTAINER
K Number
K770071
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3250
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Perkins Mfg. Co.
Date Received
January 13, 1977
Decision Date
February 24, 1977
Product Code
KDT
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
KDT Container, Specimen Mailer And Storage, Sterile

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K920550 DISPLAY PROCESSOR - MODEL IDP5100
K915232 GRUNDIG ELECTRONICS VARIOUS MODELS
K910384 VIDEO ANNOTATOR MODEL PK2310
K904986 PROGRAMMABLE VIDEO CONTROLLER MODEL PK2060
K904540 VIDEO SYSTEM INTERFACE MODELS
K896615 CINE CAMERA CONTROL MODEL PK2037
K895500 PATIENT POSITIONING ACCESSORIES
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