PLASTER CUTTING SCISSORS
K-Number: K892823 · 1989-05-25
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Device Summary
Frequently Asked Questions
What is the PLASTER CUTTING SCISSORS?
PLASTER CUTTING SCISSORS is a medical device that received FDA 510(k) clearance on 1989-05-25. The listed applicant is The South India Surgical Co. Pvt. , Ltd.. The 510(k) number is K892823.
When did PLASTER CUTTING SCISSORS receive FDA 510(k) clearance?
PLASTER CUTTING SCISSORS received FDA 510(k) clearance on 1989-05-25, under 510(k) number K892823.
Who is the listed applicant for PLASTER CUTTING SCISSORS?
The FDA 510(k) record lists The South India Surgical Co. Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLASTER CUTTING SCISSORS?
The FDA product code for PLASTER CUTTING SCISSORS is LRW.
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 The South India Surgical Co. Pvt. , 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: LRW)
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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