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FDA 510(k)

BALLARD MEDICAL PRODUCTS ELECTRO-SURG

K-Number: K820713 · 1982-03-26

ApplicantBallard Medical Products
Decision Date1982-03-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BALLARD MEDICAL PRODUCTS ELECTRO-SURG is the device name listed in this FDA 510(k) record. The listed applicant is Ballard Medical Products. It received FDA 510(k) clearance on 1982-03-26 under 510(k) number K820713. 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 BALLARD MEDICAL PRODUCTS ELECTRO-SURG?

BALLARD MEDICAL PRODUCTS ELECTRO-SURG is a medical device that received FDA 510(k) clearance on 1982-03-26. The listed applicant is Ballard Medical Products. The 510(k) number is K820713.

When did BALLARD MEDICAL PRODUCTS ELECTRO-SURG receive FDA 510(k) clearance?

BALLARD MEDICAL PRODUCTS ELECTRO-SURG received FDA 510(k) clearance on 1982-03-26, under 510(k) number K820713.

Who is the listed applicant for BALLARD MEDICAL PRODUCTS ELECTRO-SURG?

The FDA 510(k) record lists Ballard Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BALLARD MEDICAL PRODUCTS ELECTRO-SURG?

The FDA product code for BALLARD MEDICAL PRODUCTS ELECTRO-SURG is GEI.

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Other records listing Ballard Medical Products as applicant

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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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