CAM-WRAP(TM) NEW STERILIZATION PROCEDURE
K-Number: K891983 · 1989-04-19
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Device Summary
Frequently Asked Questions
What is the CAM-WRAP(TM) NEW STERILIZATION PROCEDURE?
CAM-WRAP(TM) NEW STERILIZATION PROCEDURE is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K891983.
When did CAM-WRAP(TM) NEW STERILIZATION PROCEDURE receive FDA 510(k) clearance?
CAM-WRAP(TM) NEW STERILIZATION PROCEDURE received FDA 510(k) clearance on 1989-04-19, under 510(k) number K891983.
Who is the listed applicant for CAM-WRAP(TM) NEW STERILIZATION PROCEDURE?
The FDA 510(k) record lists Medical Dynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAM-WRAP(TM) NEW STERILIZATION PROCEDURE?
The FDA product code for CAM-WRAP(TM) NEW STERILIZATION PROCEDURE is KCT.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medical Dynamics, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KCT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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