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FDA 510(k)

PRESSURE TUBING AND ACCESSORIES

K-Number: K922777 · 1994-03-22

ApplicantArbor Technologies, Inc.
Decision Date1994-03-22
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PRESSURE TUBING AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Arbor Technologies, Inc.. It received FDA 510(k) clearance on 1994-03-22 under 510(k) number K922777. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE TUBING AND ACCESSORIES?

PRESSURE TUBING AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-03-22. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K922777.

When did PRESSURE TUBING AND ACCESSORIES receive FDA 510(k) clearance?

PRESSURE TUBING AND ACCESSORIES received FDA 510(k) clearance on 1994-03-22, under 510(k) number K922777.

Who is the listed applicant for PRESSURE TUBING AND ACCESSORIES?

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

What is the FDA product code for PRESSURE TUBING AND ACCESSORIES?

The FDA product code for PRESSURE TUBING AND ACCESSORIES is HIF.

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Other records listing Arbor Technologies, Inc. as applicant

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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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