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FDA 510(k)

VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC

K-Number: K941968 · 1994-05-10

Decision Date1994-05-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1994-05-10 under 510(k) number K941968. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC?

VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC is a medical device that received FDA 510(k) clearance on 1994-05-10. The listed applicant is Valleylab, Inc.. The 510(k) number is K941968.

When did VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC receive FDA 510(k) clearance?

VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC received FDA 510(k) clearance on 1994-05-10, under 510(k) number K941968.

Who is the listed applicant for VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC?

The FDA 510(k) record lists Valleylab, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC?

The FDA product code for VALLEY MODEL E2750-T PENCIL GRIP LAPAROSCOPIC is GEI.

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 Valleylab, 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.

View all 94 devices →

Related Devices (Code: GEI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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