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FDA 510(k)

ELITE #MPS 101 ELECTROSURGICAL SWITCH

K-Number: K822070 · 1982-08-19

Decision Date1982-08-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELITE #MPS 101 ELECTROSURGICAL SWITCH is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Electronics, Inc.. It received FDA 510(k) clearance on 1982-08-19 under 510(k) number K822070. 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 ELITE #MPS 101 ELECTROSURGICAL SWITCH?

ELITE #MPS 101 ELECTROSURGICAL SWITCH is a medical device that received FDA 510(k) clearance on 1982-08-19. The listed applicant is Delta Medical Electronics, Inc.. The 510(k) number is K822070.

When did ELITE #MPS 101 ELECTROSURGICAL SWITCH receive FDA 510(k) clearance?

ELITE #MPS 101 ELECTROSURGICAL SWITCH received FDA 510(k) clearance on 1982-08-19, under 510(k) number K822070.

Who is the listed applicant for ELITE #MPS 101 ELECTROSURGICAL SWITCH?

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

What is the FDA product code for ELITE #MPS 101 ELECTROSURGICAL SWITCH?

The FDA product code for ELITE #MPS 101 ELECTROSURGICAL SWITCH 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.

Other records listing Delta Medical Electronics, 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.

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.

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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