DEROYAL SURG DISP/REUSABLE SKIN STAPLER HANDLE/CART
K-Number: K934188 · 1994-03-28
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Device Summary
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.
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
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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