WARM N WET HMEF W/LUER ADAPTER
K-Number: K953620 · 1995-08-25
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Device Summary
Frequently Asked Questions
What is the WARM N WET HMEF W/LUER ADAPTER?
WARM N WET HMEF W/LUER ADAPTER is a medical device that received FDA 510(k) clearance on 1995-08-25. The listed applicant is Hospitak, Inc.. The 510(k) number is K953620.
When did WARM N WET HMEF W/LUER ADAPTER receive FDA 510(k) clearance?
WARM N WET HMEF W/LUER ADAPTER received FDA 510(k) clearance on 1995-08-25, under 510(k) number K953620.
Who is the listed applicant for WARM N WET HMEF W/LUER ADAPTER?
The FDA 510(k) record lists Hospitak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WARM N WET HMEF W/LUER ADAPTER?
The FDA product code for WARM N WET HMEF W/LUER ADAPTER is BYD.
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 Hospitak, 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: BYD)
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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