WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE
K-Number: K904999 · 1993-01-26
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Device Summary
Frequently Asked Questions
What is the WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE?
WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE is a medical device that received FDA 510(k) clearance on 1993-01-26. The listed applicant is Opticon Medical, Inc.. The 510(k) number is K904999.
When did WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE receive FDA 510(k) clearance?
WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE received FDA 510(k) clearance on 1993-01-26, under 510(k) number K904999.
Who is the listed applicant for WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE?
The FDA 510(k) record lists Opticon Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE?
The FDA product code for WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE is BSR.
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 Opticon Medical, 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: BSR)
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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