STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS
K-Number: K102752 · 2011-11-09
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Device Summary
Frequently Asked Questions
What is the STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS?
STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 2011-11-09. The listed applicant is Stingray Surgical Products, Inc.. The 510(k) number is K102752.
When did STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS receive FDA 510(k) clearance?
STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS received FDA 510(k) clearance on 2011-11-09, under 510(k) number K102752.
Who is the listed applicant for STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS?
The FDA 510(k) record lists Stingray Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS?
The FDA product code for STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPS is GEI.
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 Stingray Surgical Products, 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: GEI)
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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