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FDA 510(k)

R2 ELECTROSURG. RETURN ELECT. #225ETC.

K-Number: K800933 · 1980-05-20

ApplicantR2 Corp.
Decision Date1980-05-20
Product CodeJOT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

R2 ELECTROSURG. RETURN ELECT. #225ETC. is the device name listed in this FDA 510(k) record. The listed applicant is R2 Corp.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K800933. The device is classified under product code JOT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R2 ELECTROSURG. RETURN ELECT. #225ETC.?

R2 ELECTROSURG. RETURN ELECT. #225ETC. is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is R2 Corp.. The 510(k) number is K800933.

When did R2 ELECTROSURG. RETURN ELECT. #225ETC. receive FDA 510(k) clearance?

R2 ELECTROSURG. RETURN ELECT. #225ETC. received FDA 510(k) clearance on 1980-05-20, under 510(k) number K800933.

Who is the listed applicant for R2 ELECTROSURG. RETURN ELECT. #225ETC.?

The FDA 510(k) record lists R2 Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R2 ELECTROSURG. RETURN ELECT. #225ETC.?

The FDA product code for R2 ELECTROSURG. RETURN ELECT. #225ETC. is JOT.

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Other records listing R2 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.

K832516MAGNATRODE CARDIAC MONITORING ELECTRODEK800932ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120K800936R2 PADDLE TYPE CABLE-ADAPTOR #S 170,171K800935R2 APEX-POST.,ANT.&POST. ELECT.(12 MODS)K800930R2(TM) ECG ELECTRODE SET-#'S305-306 ETC.K800937R2 PLATE TYPE CABLE-ADAPTOR #S 175,176

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Related Devices (Code: JOT)

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.

K923647RFG-DGP DISPOSABLE GROUNDING PADSRadionics, Inc.K905545ULTRASOUND TRANSMISSION GELArbo Medical, Inc.K904418ULTRASOUND COUPLING GELGeno LaboratoriesK901217TRIA-SONIC ULTRA SOUND TRANSMISSION GELH & P Industries, Inc.K894490STERILE ULTRASOUND TRANSMISSION GELSwedish Trade Council USAK884503ULTRASONIC TRANSMISSION GELHerbert Stanley Co.

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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