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FDA 510(k)

STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG

K-Number: K934165 · 1994-01-25

ApplicantPhx Technologies Corp.
Decision Date1994-01-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG is the device name listed in this FDA 510(k) record. The listed applicant is Phx Technologies Corp.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K934165. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG?

STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Phx Technologies Corp.. The 510(k) number is K934165.

When did STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG receive FDA 510(k) clearance?

STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG received FDA 510(k) clearance on 1994-01-25, under 510(k) number K934165.

Who is the listed applicant for STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG?

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

What is the FDA product code for STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG?

The FDA product code for STERILE, DISPOSABLE ENDO SPECIEMEN RETRIEVAL BAG is GCJ.

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Related Devices (Code: GCJ)

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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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