LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)
K-Number: K925079 · 1994-08-24
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Device Summary
Frequently Asked Questions
What is the LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)?
LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER) is a medical device that received FDA 510(k) clearance on 1994-08-24. The listed applicant is Endo Technic Corp.. The 510(k) number is K925079.
When did LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER) receive FDA 510(k) clearance?
LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER) received FDA 510(k) clearance on 1994-08-24, under 510(k) number K925079.
Who is the listed applicant for LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)?
The FDA 510(k) record lists Endo Technic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)?
The FDA product code for LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER) is HET.
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 Endo Technic 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: HET)
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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