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FDA 510(k)

INSUFFLATOR TUBING WITH FILTER

K-Number: K943508 · 1994-11-17

ApplicantStryker Endoscopy
Decision Date1994-11-17
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INSUFFLATOR TUBING WITH FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1994-11-17 under 510(k) number K943508. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSUFFLATOR TUBING WITH FILTER?

INSUFFLATOR TUBING WITH FILTER is a medical device that received FDA 510(k) clearance on 1994-11-17. The listed applicant is Stryker Endoscopy. The 510(k) number is K943508.

When did INSUFFLATOR TUBING WITH FILTER receive FDA 510(k) clearance?

INSUFFLATOR TUBING WITH FILTER received FDA 510(k) clearance on 1994-11-17, under 510(k) number K943508.

Who is the listed applicant for INSUFFLATOR TUBING WITH FILTER?

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

What is the FDA product code for INSUFFLATOR TUBING WITH FILTER?

The FDA product code for INSUFFLATOR TUBING WITH FILTER is HET.

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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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