FDA 510(k) Premarket Notification K962045: ANESTHESIA BREATHING CIRCUIT/ANESTHESIA BREATHING KIT

Submission Details & Decision

Normalized public record details for 510(k) notification K962045.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K962045

Applicant / Sponsor

Mallinckrodt Medical

Device Name

ANESTHESIA BREATHING CIRCUIT/ANESTHESIA BREATHING KIT

Product Code

CAH

Decision Date

1996-11-26

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Anesthesiology (AN)

Clearance Type

Traditional

Third Party Flag

Date Received

1996-05-28

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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 Information may be outdated or incomplete.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.