DIAMOND-SHARP(R) TROCARS
K-Number: K924148 · 1994-02-28
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Device Summary
Frequently Asked Questions
What is the DIAMOND-SHARP(R) TROCARS?
DIAMOND-SHARP(R) TROCARS is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Snowden-Pencer. The 510(k) number is K924148.
When did DIAMOND-SHARP(R) TROCARS receive FDA 510(k) clearance?
DIAMOND-SHARP(R) TROCARS received FDA 510(k) clearance on 1994-02-28, under 510(k) number K924148.
Who is the listed applicant for DIAMOND-SHARP(R) TROCARS?
The FDA 510(k) record lists Snowden-Pencer as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAMOND-SHARP(R) TROCARS?
The FDA product code for DIAMOND-SHARP(R) TROCARS is HFI.
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 Snowden-Pencer 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: HFI)
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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