LIFESHIELD ANESTHESIA SET
K-Number: K913982 · 1992-11-05
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Device Summary
Frequently Asked Questions
What is the LIFESHIELD ANESTHESIA SET?
LIFESHIELD ANESTHESIA SET is a medical device that received FDA 510(k) clearance on 1992-11-05. The listed applicant is Abbott Laboratories. The 510(k) number is K913982.
When did LIFESHIELD ANESTHESIA SET receive FDA 510(k) clearance?
LIFESHIELD ANESTHESIA SET received FDA 510(k) clearance on 1992-11-05, under 510(k) number K913982.
Who is the listed applicant for LIFESHIELD ANESTHESIA SET?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIFESHIELD ANESTHESIA SET?
The FDA product code for LIFESHIELD ANESTHESIA SET is FPA.
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 Abbott Laboratories 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: FPA)
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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