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FDA 510(k)

DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART

K-Number: K934188 · 1994-03-28

Decision Date1994-03-28
Product CodeGAG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART 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 1994-03-28 under 510(k) number K934188. The device is classified under product code GAG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART?

DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K934188.

When did DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART receive FDA 510(k) clearance?

DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART received FDA 510(k) clearance on 1994-03-28, under 510(k) number K934188.

Who is the listed applicant for DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART?

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 SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART?

The FDA product code for DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART is GAG.

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.

View all 90 devices →

Related Devices (Code: GAG)

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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