INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS
K-Number: K940718 · 1994-07-22
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Device Summary
Frequently Asked Questions
What is the INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS?
INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-07-22. The listed applicant is Innervision, Inc.. The 510(k) number is K940718.
When did INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS receive FDA 510(k) clearance?
INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS received FDA 510(k) clearance on 1994-07-22, under 510(k) number K940718.
Who is the listed applicant for INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS?
The FDA 510(k) record lists Innervision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS?
The FDA product code for INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS 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 Innervision, Inc. 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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