ANESTHESIA APATATUS #D-25
K-Number: K830161 · 1983-03-09
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Device Summary
Frequently Asked Questions
What is the ANESTHESIA APATATUS #D-25?
ANESTHESIA APATATUS #D-25 is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is W.E. Leder Enterprises, Inc.. The 510(k) number is K830161.
When did ANESTHESIA APATATUS #D-25 receive FDA 510(k) clearance?
ANESTHESIA APATATUS #D-25 received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830161.
Who is the listed applicant for ANESTHESIA APATATUS #D-25?
The FDA 510(k) record lists W.E. Leder Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANESTHESIA APATATUS #D-25?
The FDA product code for ANESTHESIA APATATUS #D-25 is BSZ.
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 W.E. Leder Enterprises, 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: BSZ)
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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