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FDA 510(k)

ELECTROSURGICAL GROUNDING PAD

K-Number: K772160 · 1977-11-28

ApplicantNdm Corp.
Decision Date1977-11-28
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL GROUNDING PAD is the device name listed in this FDA 510(k) record. The listed applicant is Ndm Corp.. It received FDA 510(k) clearance on 1977-11-28 under 510(k) number K772160. 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 ELECTROSURGICAL GROUNDING PAD?

ELECTROSURGICAL GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is Ndm Corp.. The 510(k) number is K772160.

When did ELECTROSURGICAL GROUNDING PAD receive FDA 510(k) clearance?

ELECTROSURGICAL GROUNDING PAD received FDA 510(k) clearance on 1977-11-28, under 510(k) number K772160.

Who is the listed applicant for ELECTROSURGICAL GROUNDING PAD?

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

What is the FDA product code for ELECTROSURGICAL GROUNDING PAD?

The FDA product code for ELECTROSURGICAL GROUNDING PAD is JOS.

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Other records listing Ndm 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.

K926202CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSIK901145NDM SWITCHPEN HOLSTERK853968DIATEMP ELECTROSURGICAL PENK830663PENCIL SKIN ABRADERK810920NDM DIATEMP INFANT ELECTROSURG. DISP. P.K801158NDM DIATEMP ELECTROSURGICAL DIS. PAD

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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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