INSUFFLATOR TUBING KIT W/FILTER
K-Number: K933094 · 1994-04-18
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Device Summary
Frequently Asked Questions
What is the INSUFFLATOR TUBING KIT W/FILTER?
INSUFFLATOR TUBING KIT W/FILTER is a medical device that received FDA 510(k) clearance on 1994-04-18. The listed applicant is Inman Medical Corp.. The 510(k) number is K933094.
When did INSUFFLATOR TUBING KIT W/FILTER receive FDA 510(k) clearance?
INSUFFLATOR TUBING KIT W/FILTER received FDA 510(k) clearance on 1994-04-18, under 510(k) number K933094.
Who is the listed applicant for INSUFFLATOR TUBING KIT W/FILTER?
The FDA 510(k) record lists Inman Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSUFFLATOR TUBING KIT W/FILTER?
The FDA product code for INSUFFLATOR TUBING KIT W/FILTER is HIF.
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 Inman Medical Corp. 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: HIF)
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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