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FDA 510(k)

DISPOSABLE ELECTRODE

K-Number: K820664 · 1982-03-19

ApplicantTrident Surgical Corp.
Decision Date1982-03-19
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Trident Surgical Corp.. It received FDA 510(k) clearance on 1982-03-19 under 510(k) number K820664. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE ELECTRODE?

DISPOSABLE ELECTRODE is a medical device that received FDA 510(k) clearance on 1982-03-19. The listed applicant is Trident Surgical Corp.. The 510(k) number is K820664.

When did DISPOSABLE ELECTRODE receive FDA 510(k) clearance?

DISPOSABLE ELECTRODE received FDA 510(k) clearance on 1982-03-19, under 510(k) number K820664.

Who is the listed applicant for DISPOSABLE ELECTRODE?

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

What is the FDA product code for DISPOSABLE ELECTRODE?

The FDA product code for DISPOSABLE ELECTRODE is HAM.

Related Clinical Trials

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.

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Other records listing Trident Surgical 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.

K812769TRIDENT #2001

Related Devices (Code: HAM)

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.

K153472Quiver Laparoscopic ExtendableItl Corporation Pty, Ltd.K000079NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777MNikomed U.S.A., Inc.K993306NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)Paladin Medical, Inc.K945861BERGEN 710 ESUBergen Mfg.K913300LAPAROSTAT(TM)Cook Ob/GynK920100GSU HANDPIECE ADAPTERBeacon Laboratories, 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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