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FDA 510(k)

DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING

K-Number: K934131 · 1994-03-07

Decision Date1994-03-07
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K934131. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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