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FDA 510(k)

PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228

K-Number: K003249 · 2000-12-12

ApplicantPst, Inc.
Decision Date2000-12-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228 is the device name listed in this FDA 510(k) record. The listed applicant is Pst, Inc.. It received FDA 510(k) clearance on 2000-12-12 under 510(k) number K003249. 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 PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228?

PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228 is a medical device that received FDA 510(k) clearance on 2000-12-12. The listed applicant is Pst, Inc.. The 510(k) number is K003249.

When did PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228 receive FDA 510(k) clearance?

PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228 received FDA 510(k) clearance on 2000-12-12, under 510(k) number K003249.

Who is the listed applicant for PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228?

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

What is the FDA product code for PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228?

The FDA product code for PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228 is GEI.

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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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