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FDA 510(k)

PENCIL, ELECTROSURGICAL

K-Number: K760168 · 1976-08-09

ApplicantDytek Corp.
Decision Date1976-08-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PENCIL, ELECTROSURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Dytek Corp.. It received FDA 510(k) clearance on 1976-08-09 under 510(k) number K760168. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENCIL, ELECTROSURGICAL?

PENCIL, ELECTROSURGICAL is a medical device that received FDA 510(k) clearance on 1976-08-09. The listed applicant is Dytek Corp.. The 510(k) number is K760168.

When did PENCIL, ELECTROSURGICAL receive FDA 510(k) clearance?

PENCIL, ELECTROSURGICAL received FDA 510(k) clearance on 1976-08-09, under 510(k) number K760168.

Who is the listed applicant for PENCIL, ELECTROSURGICAL?

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

What is the FDA product code for PENCIL, ELECTROSURGICAL?

The FDA product code for PENCIL, ELECTROSURGICAL is GEI.

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 Dytek 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.

K781245LUNG EXER. BAG, POST-OP, MODIFIEDK760167BAG, POST OPERATIVE LUNG EXERCIZING BLOW

Related Devices (Code: GEI)

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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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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