DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING
K-Number: K934131 · 1994-03-07
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Device Summary
Frequently Asked Questions
What is the DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING?
DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K934131.
When did DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING receive FDA 510(k) clearance?
DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING received FDA 510(k) clearance on 1994-03-07, under 510(k) number K934131.
Who is the listed applicant for DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING?
The FDA 510(k) record lists Deroyal Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING?
The FDA product code for DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING 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 Deroyal Industries, 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: 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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