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FDA 510(k)

PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)

K-Number: K970418 · 1997-04-29

ApplicantPmt Corp.
Decision Date1997-04-29
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX) is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corp.. It received FDA 510(k) clearance on 1997-04-29 under 510(k) number K970418. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)?

PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX) is a medical device that received FDA 510(k) clearance on 1997-04-29. The listed applicant is Pmt Corp.. The 510(k) number is K970418.

When did PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX) receive FDA 510(k) clearance?

PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX) received FDA 510(k) clearance on 1997-04-29, under 510(k) number K970418.

Who is the listed applicant for PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)?

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 PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)?

The FDA product code for PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX) is GZL.

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Other records listing Pmt Corp. as applicant

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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: GZL)

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.

K253970Wovyn Depth ElectrodeSensomedical Labs, Ltd.K250363Depth Electrode (RSDE-08); Depth Electrode (RSDE-10); Depth Electrode (RSDE-12); Depth Electrode (RSDE-14); Depth Electrode (RSDE-16); Depth Electrode (RSDE-16F); Depth Electrode (RSDE-08S); Depth Electrode (RSDE-10S); Depth Electrode (RSDE-12S); Depth Electrode (RSDE-14S); Depth Electrode (RSDE-16S); Depth Electrode (RSDE-16G); Depth Electrode (RSDE-18); Depth Electrode (RSDE-18F); Depth Electrode (RSDE-18T); Depth Electrode (RSDE-20); Depth Electrode (RSDE-20F); DeptBeijing Sinovation Medical Technology Co., Ltd.K250601Neuro Omega System; NeuroSmart SystemAlpha Omega Engineering , Ltd.K223276Anchor Bolts as Accessories to Depth ElectrodesAd-Tech Medical Instrument CorporationK223269Spencer Probe Depth ElectrodesAd-Tech Medical Instrument CorporationK213170SENSOSEEG Depth ElectrodesSensomedical Labs, Ltd.

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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