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FDA 510(k)

MODEL 80-1983, ELECTROSURGICAL GENERATOR

K-Number: K931437 · 1994-05-27

ApplicantCameron-Miller, Inc.
Decision Date1994-05-27
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL 80-1983, ELECTROSURGICAL GENERATOR 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 1994-05-27 under 510(k) number K931437. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 80-1983, ELECTROSURGICAL GENERATOR?

MODEL 80-1983, ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 1994-05-27. The listed applicant is Cameron-Miller, Inc.. The 510(k) number is K931437.

When did MODEL 80-1983, ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

MODEL 80-1983, ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 1994-05-27, under 510(k) number K931437.

Who is the listed applicant for MODEL 80-1983, ELECTROSURGICAL GENERATOR?

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 MODEL 80-1983, ELECTROSURGICAL GENERATOR?

The FDA product code for MODEL 80-1983, ELECTROSURGICAL GENERATOR is HGI.

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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 GENERATORK935490ELECTROSURGICAL DEVICE, MODEL 26-2500K854109ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345K853972CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATORK833449HAND CONTROLLED PENCIL OR SWITCH HAND

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Related Devices (Code: HGI)

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.

K202915IRIS Thermocoagulator and Digital ColposcopeLiger Medical, LLCK152843Liger Medical HTU-110Liger Medical, LLCK121881DOMAIN SURGICAL SYSTEMDomain Surgical, Inc.K070877ENDOCERVICAL ELECTRODE # 2Modern Medical Equipment Mfg., Ltd.K061651FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158Apple Medical Corp.K022593THOMAS MEDICAL ELECTRODESThomas Medical, Inc.

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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