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FDA 510(k)

ELECTROSURGICAL UNIT 75

K-Number: K781101 · 1978-07-17

ApplicantRitter Co.
Decision Date1978-07-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL UNIT 75 is the device name listed in this FDA 510(k) record. The listed applicant is Ritter Co.. It received FDA 510(k) clearance on 1978-07-17 under 510(k) number K781101. 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 UNIT 75?

ELECTROSURGICAL UNIT 75 is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Ritter Co.. The 510(k) number is K781101.

When did ELECTROSURGICAL UNIT 75 receive FDA 510(k) clearance?

ELECTROSURGICAL UNIT 75 received FDA 510(k) clearance on 1978-07-17, under 510(k) number K781101.

Who is the listed applicant for ELECTROSURGICAL UNIT 75?

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

What is the FDA product code for ELECTROSURGICAL UNIT 75?

The FDA product code for ELECTROSURGICAL UNIT 75 is GEI.

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Other records listing Ritter Co. 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.

K831245TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANOK832171SELF CHECK DIGITAL BLOOD PRESS. MONITORK831976POWER OPTICK823180SA-21 DENTAL UNITK800084RITTER MODEL J DENTAL CHAIRK780293ELECTROSURGICAL UNIT

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Related Devices (Code: GEI)

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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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