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FDA 510(k)

ELECTROCAUTERY SYSTEM MODEL 1980

K-Number: K933079 · 1994-02-22

ApplicantPmt Corp.
Decision Date1994-02-22
Product CodeHQP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ELECTROCAUTERY SYSTEM MODEL 1980 is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corp.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K933079. The device is classified under product code HQP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROCAUTERY SYSTEM MODEL 1980?

ELECTROCAUTERY SYSTEM MODEL 1980 is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Pmt Corp.. The 510(k) number is K933079.

When did ELECTROCAUTERY SYSTEM MODEL 1980 receive FDA 510(k) clearance?

ELECTROCAUTERY SYSTEM MODEL 1980 received FDA 510(k) clearance on 1994-02-22, under 510(k) number K933079.

Who is the listed applicant for ELECTROCAUTERY SYSTEM MODEL 1980?

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

What is the FDA product code for ELECTROCAUTERY SYSTEM MODEL 1980?

The FDA product code for ELECTROCAUTERY SYSTEM MODEL 1980 is HQP.

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Other records listing Pmt 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.

K122376PMT TRUSCAN SURFACE ELECTRODEK090733PMT HALO SYSTEMK082474PMT SUBDURAL CORTICAL ELECTRODESK042901ENDOMARK STERILE INDIA INKK033730PMT SPHENOIDAL ELECTRODE AND ACCESSORY, MODEL 2101-31 AND 2102-31 SERIESK972597PMT NEW BEGINNINGS GELSHAPES & AMEND

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Related Devices (Code: HQP)

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.

K121441CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP)Bovie Medical CorporationK083428F7244, F7255, F7266, F7277, F7288, F7233, F7234 SERIES OF BATTERY-POWERED CAUTERYFiab SpaK062659KIRWAN DISPOSABLE BATTERY-POWERED CAUTERY, MODEL 41-61XX SERIESKirwan Surgical Products, Inc.K023506SURGICAL MEDICAL DEVICE CAUTERYModern Medical Equipment Mfg., Ltd.K002547STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTORStarion InstrumentsK994019CAUTERY GRASPER/DISSECTORStarion Instruments

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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