Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:United_States_federal_law
|
| gptkbp:amendedBy |
gptkb:Federal_Food,_Drug,_and_Cosmetic_Act
|
| gptkbp:country |
gptkb:United_States
|
| gptkbp:dateEnacted |
1976-05-28
|
| gptkbp:enactedBy |
gptkb:United_States_Congress
|
| https://www.w3.org/2000/01/rdf-schema#label |
Public Law 94-295
|
| gptkbp:providesFor |
postmarket surveillance
premarket approval performance standards medical device reporting classification of medical devices |
| gptkbp:publicLawNumber |
94-295
|
| gptkbp:shortName |
gptkb:Medical_Device_Amendments_of_1976
|
| gptkbp:signedBy |
gptkb:Gerald_Ford
|
| gptkbp:statutesAtLargeCitation |
90 Stat. 539
|
| gptkbp:subject |
medical devices regulation
FDA authority |
| gptkbp:bfsParent |
gptkb:Medical_Device_Amendments_of_1976
|
| gptkbp:bfsLayer |
7
|