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FDA 510(k)

PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE

K-Number: K882793 · 1988-07-18

ApplicantPmt Corp.
Decision Date1988-07-18
Product CodeGAF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corp.. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K882793. The device is classified under product code GAF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE?

PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Pmt Corp.. The 510(k) number is K882793.

When did PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE receive FDA 510(k) clearance?

PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882793.

Who is the listed applicant for PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE?

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 FUKUSHIMA MICROSURGICAL INSTRUMENT LINE?

The FDA product code for PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE is GAF.

Related Clinical Trials

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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: GAF)

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.

K023688LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPERLeMaitre Vascular, Inc.K935357SNAP RECIPROCATING SAWSurgiquip, Inc.K890374ABDOMINAL SPATULAKinetic Medical ProductsK822108CEMENT-PICKBio-Blitz, Inc.

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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