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FDA 510(k)

INFANT ELECTROSURGICAL GROUNDING PAD

K-Number: K780405 · 1978-04-05

ApplicantNew Dimensions IN Medicine, Inc.
Decision Date1978-04-05
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INFANT ELECTROSURGICAL GROUNDING PAD is the device name listed in this FDA 510(k) record. The listed applicant is New Dimensions IN Medicine, Inc.. It received FDA 510(k) clearance on 1978-04-05 under 510(k) number K780405. 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 INFANT ELECTROSURGICAL GROUNDING PAD?

INFANT ELECTROSURGICAL GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1978-04-05. The listed applicant is New Dimensions IN Medicine, Inc.. The 510(k) number is K780405.

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

INFANT ELECTROSURGICAL GROUNDING PAD received FDA 510(k) clearance on 1978-04-05, under 510(k) number K780405.

Who is the listed applicant for INFANT ELECTROSURGICAL GROUNDING PAD?

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

What is the FDA product code for INFANT ELECTROSURGICAL GROUNDING PAD?

The FDA product code for INFANT ELECTROSURGICAL GROUNDING PAD is JOS.

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Other records listing New Dimensions IN Medicine, 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.

K920677CLEARSITE HYDROGEL WOUND DRESSING MODIFICATIONK832145MONOBLOCK PROSTOPERATIVE TENS ELECTRODEK822077RESPIRATION MONITOR TYPE MR-10K780631NDM INFANT ECG PACKPADK771749AMALGAM DISPENSER

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

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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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