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FDA 510(k)

ELIMINATOR #BPS 201 BIPOLAR ELECTRO

K-Number: K822069 · 1982-08-19

ApplicantDelta Medical Electronics, Inc.
Decision Date1982-08-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELIMINATOR #BPS 201 BIPOLAR ELECTRO 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 K822069. 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 ELIMINATOR #BPS 201 BIPOLAR ELECTRO?

ELIMINATOR #BPS 201 BIPOLAR ELECTRO 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 K822069.

When did ELIMINATOR #BPS 201 BIPOLAR ELECTRO receive FDA 510(k) clearance?

ELIMINATOR #BPS 201 BIPOLAR ELECTRO received FDA 510(k) clearance on 1982-08-19, under 510(k) number K822069.

Who is the listed applicant for ELIMINATOR #BPS 201 BIPOLAR ELECTRO?

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 ELIMINATOR #BPS 201 BIPOLAR ELECTRO?

The FDA product code for ELIMINATOR #BPS 201 BIPOLAR ELECTRO 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 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.

K832157DELTA CONDUCTIVE ADHESIVE ELECTROSURG-K831299EVEN-TEMP. CAPACITIVE ADHESIVE PADK822070ELITE #MPS 101 ELECTROSURGICAL SWITCH

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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