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ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982073
510(k) Type
Traditional
Applicant
Anchor Products Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1998
Days to Decision
102 days
Submission Type
Statement

ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982073
510(k) Type
Traditional
Applicant
Anchor Products Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1998
Days to Decision
102 days
Submission Type
Statement