KEYSTONE OXYGEN TENT
K-Number: K893714 · 1989-08-21
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Device Summary
Frequently Asked Questions
What is the KEYSTONE OXYGEN TENT?
KEYSTONE OXYGEN TENT is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Keystone Veterinary Supplies, Inc.. The 510(k) number is K893714.
When did KEYSTONE OXYGEN TENT receive FDA 510(k) clearance?
KEYSTONE OXYGEN TENT received FDA 510(k) clearance on 1989-08-21, under 510(k) number K893714.
Who is the listed applicant for KEYSTONE OXYGEN TENT?
The FDA 510(k) record lists Keystone Veterinary Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KEYSTONE OXYGEN TENT?
The FDA product code for KEYSTONE OXYGEN TENT is BYL.
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 Keystone Veterinary Supplies, 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: BYL)
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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