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FDA 510(k)

STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230

K-Number: K994173 · 2000-01-20

ApplicantStellartech Research Corp.
Decision Date2000-01-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230 is the device name listed in this FDA 510(k) record. The listed applicant is Stellartech Research Corp.. It received FDA 510(k) clearance on 2000-01-20 under 510(k) number K994173. 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 STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230?

STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230 is a medical device that received FDA 510(k) clearance on 2000-01-20. The listed applicant is Stellartech Research Corp.. The 510(k) number is K994173.

When did STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230 receive FDA 510(k) clearance?

STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230 received FDA 510(k) clearance on 2000-01-20, under 510(k) number K994173.

Who is the listed applicant for STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230?

The FDA 510(k) record lists Stellartech Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230?

The FDA product code for STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230 is GEI.

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Other records listing Stellartech Research Corp. 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.

K061544STELLARTECH 100 COAGULATION SYSTEMK050831STELLARTECH COAGULATION SYSTEM 2, MODELS 1100C-115A AND 1100C-230AK042909STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115A & 1100C-230AK041383STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 AND 1100C-230K040240STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)K032721MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)

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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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