SUTURE CUTTER
K-Number: K780574 · 1978-07-17
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Device Summary
Frequently Asked Questions
What is the SUTURE CUTTER?
SUTURE CUTTER is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Laschal Instrument Corp.. The 510(k) number is K780574.
When did SUTURE CUTTER receive FDA 510(k) clearance?
SUTURE CUTTER received FDA 510(k) clearance on 1978-07-17, under 510(k) number K780574.
Who is the listed applicant for SUTURE CUTTER?
The FDA 510(k) record lists Laschal Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUTURE CUTTER?
The FDA product code for SUTURE CUTTER is FZT.
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 Laschal Instrument Corp. 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: FZT)
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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