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FDA 510(k)

CONICAL OBTURATOR

K-Number: K954459 · 1995-10-23

ApplicantPhx Technologies Corp.
Decision Date1995-10-23
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONICAL OBTURATOR 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 1995-10-23 under 510(k) number K954459. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONICAL OBTURATOR?

CONICAL OBTURATOR is a medical device that received FDA 510(k) clearance on 1995-10-23. The listed applicant is Phx Technologies Corp.. The 510(k) number is K954459.

When did CONICAL OBTURATOR receive FDA 510(k) clearance?

CONICAL OBTURATOR received FDA 510(k) clearance on 1995-10-23, under 510(k) number K954459.

Who is the listed applicant for CONICAL OBTURATOR?

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 CONICAL OBTURATOR?

The FDA product code for CONICAL OBTURATOR is HRX.

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Other records listing Phx Technologies Corp. as applicant

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Related Devices (Code: HRX)

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.

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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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