SCALP VEIN SETS
K-Number: K772008 · 1978-01-03
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Device Summary
Frequently Asked Questions
What is the SCALP VEIN SETS?
SCALP VEIN SETS is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Suru Chemicals & Pharmaceuticals, Ltd.. The 510(k) number is K772008.
When did SCALP VEIN SETS receive FDA 510(k) clearance?
SCALP VEIN SETS received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772008.
Who is the listed applicant for SCALP VEIN SETS?
The FDA 510(k) record lists Suru Chemicals & Pharmaceuticals, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCALP VEIN SETS?
The FDA product code for SCALP VEIN SETS is FPA.
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 Suru Chemicals & Pharmaceuticals, Ltd. 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: FPA)
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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