OXYGEN TUBING, 81503
K-Number: K913422 · 1992-01-30
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Device Summary
Frequently Asked Questions
What is the OXYGEN TUBING, 81503?
OXYGEN TUBING, 81503 is a medical device that received FDA 510(k) clearance on 1992-01-30. The listed applicant is Specialty Packaging Producs, Inc.. The 510(k) number is K913422.
When did OXYGEN TUBING, 81503 receive FDA 510(k) clearance?
OXYGEN TUBING, 81503 received FDA 510(k) clearance on 1992-01-30, under 510(k) number K913422.
Who is the listed applicant for OXYGEN TUBING, 81503?
The FDA 510(k) record lists Specialty Packaging Producs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYGEN TUBING, 81503?
The FDA product code for OXYGEN TUBING, 81503 is BYX.
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 Specialty Packaging Producs, 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: BYX)
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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