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FDA 510(k)

ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345

K-Number: K854109 · 1986-01-24

ApplicantCameron-Miller, Inc.
Decision Date1986-01-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345 is the device name listed in this FDA 510(k) record. The listed applicant is Cameron-Miller, Inc.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K854109. 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 ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345?

ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345 is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Cameron-Miller, Inc.. The 510(k) number is K854109.

When did ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345 receive FDA 510(k) clearance?

ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345 received FDA 510(k) clearance on 1986-01-24, under 510(k) number K854109.

Who is the listed applicant for ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345?

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

What is the FDA product code for ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345?

The FDA product code for ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345 is GEI.

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Other records listing Cameron-Miller, 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.

K944775ELECTROSURGICAL UNIT MODEL 26-0335K931541MODEL 26-0375, ELECTROSURGICAL GENERATORK931437MODEL 80-1983, ELECTROSURGICAL GENERATORK935490ELECTROSURGICAL DEVICE, MODEL 26-2500K853972CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATORK833449HAND CONTROLLED PENCIL OR SWITCH HAND

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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.

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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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