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FDA 510(k)

MONOPOLAR CAUTERY BLADE TIP #TM-1701

K-Number: K873653 · 1987-12-15

ApplicantArthropedics, Inc.
Decision Date1987-12-15
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MONOPOLAR CAUTERY BLADE TIP #TM-1701 is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1987-12-15 under 510(k) number K873653. The device is classified under product code JOS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOPOLAR CAUTERY BLADE TIP #TM-1701?

MONOPOLAR CAUTERY BLADE TIP #TM-1701 is a medical device that received FDA 510(k) clearance on 1987-12-15. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873653.

When did MONOPOLAR CAUTERY BLADE TIP #TM-1701 receive FDA 510(k) clearance?

MONOPOLAR CAUTERY BLADE TIP #TM-1701 received FDA 510(k) clearance on 1987-12-15, under 510(k) number K873653.

Who is the listed applicant for MONOPOLAR CAUTERY BLADE TIP #TM-1701?

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

What is the FDA product code for MONOPOLAR CAUTERY BLADE TIP #TM-1701?

The FDA product code for MONOPOLAR CAUTERY BLADE TIP #TM-1701 is JOS.

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Other records listing Arthropedics, Inc. 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.

K873619ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)K873655MONOPOLAR CAUTERY RETROGADE TIP #TM-1703K873654MONOPOLAR CAUTERY CONICAL TIP #TM-1702K873387VIDEO ARTHROSCOPE, 1.7MM X 55 MMK873651BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375K873711RETROGRADE KNIFE, DISPOSABLE #TM-1613

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Related Devices (Code: JOS)

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.

K161600Resection ElectrodesOlympus Winter & Ibe GmbHK050923LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATORConmed LinvatecK012684REPROCESSED ELECTROSURGICAL ELECTRODESterilmed, Inc.K011515MEDLINE GROUNDING PADMedline Industries, Inc.K003403ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999Highland / Marietta, Inc.K000333STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MODTriad Surgical Technologies, 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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