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GOETTINGER EMERGENCY RESUSCITATION TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892123
510(k) Type
Traditional
Applicant
PLASTIC PARTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
102 days

GOETTINGER EMERGENCY RESUSCITATION TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892123
510(k) Type
Traditional
Applicant
PLASTIC PARTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
102 days