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FDA 510(k)

SUOP ELECTRODES FOR EXCISIONAL PROCEDURES

K-Number: K921386 · 1993-10-08

ApplicantSilver Creek Surgical
Decision Date1993-10-08
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SUOP ELECTRODES FOR EXCISIONAL PROCEDURES is the device name listed in this FDA 510(k) record. The listed applicant is Silver Creek Surgical. It received FDA 510(k) clearance on 1993-10-08 under 510(k) number K921386. 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 SUOP ELECTRODES FOR EXCISIONAL PROCEDURES?

SUOP ELECTRODES FOR EXCISIONAL PROCEDURES is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Silver Creek Surgical. The 510(k) number is K921386.

When did SUOP ELECTRODES FOR EXCISIONAL PROCEDURES receive FDA 510(k) clearance?

SUOP ELECTRODES FOR EXCISIONAL PROCEDURES received FDA 510(k) clearance on 1993-10-08, under 510(k) number K921386.

Who is the listed applicant for SUOP ELECTRODES FOR EXCISIONAL PROCEDURES?

The FDA 510(k) record lists Silver Creek Surgical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUOP ELECTRODES FOR EXCISIONAL PROCEDURES?

The FDA product code for SUOP ELECTRODES FOR EXCISIONAL PROCEDURES is HGI.

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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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