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FDA 510(k)

NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS

K-Number: K951731 · 1995-05-16

Decision Date1995-05-16
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS is the device name listed in this FDA 510(k) record. The listed applicant is American Hydro-Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1995-05-16 under 510(k) number K951731. 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 NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS?

NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS is a medical device that received FDA 510(k) clearance on 1995-05-16. The listed applicant is American Hydro-Surgical Instruments, Inc.. The 510(k) number is K951731.

When did NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS receive FDA 510(k) clearance?

NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS received FDA 510(k) clearance on 1995-05-16, under 510(k) number K951731.

Who is the listed applicant for NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS?

The FDA 510(k) record lists American Hydro-Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS?

The FDA product code for NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS 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 American Hydro-Surgical Instruments, 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 18 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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