BONE MARROW ASPIRATION KIT

FDA 510(k) Premarket Notification · Submission K781371 · Applicant: Ferris Mfg. Corp.

Public Record 510(k) Submission Decision Date: 1978-09-20 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K781371.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K781371
Applicant / Sponsor
Device Name
BONE MARROW ASPIRATION KIT
Product Code
GAA
Decision Date
1978-09-20
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1978-08-08

Related Establishments / Registrations

Public Record Disclaimer

This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.

Account Required Full available specs will require a free AvaSpecs account.