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FDA 510(k)

INSUFFLATOR TUBING

K-Number: K872860 · 1987-11-16

ApplicantMedline Industries, Inc.
Decision Date1987-11-16
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INSUFFLATOR TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1987-11-16 under 510(k) number K872860. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSUFFLATOR TUBING?

INSUFFLATOR TUBING is a medical device that received FDA 510(k) clearance on 1987-11-16. The listed applicant is Medline Industries, Inc.. The 510(k) number is K872860.

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

INSUFFLATOR TUBING received FDA 510(k) clearance on 1987-11-16, under 510(k) number K872860.

Who is the listed applicant for INSUFFLATOR TUBING?

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

What is the FDA product code for INSUFFLATOR TUBING?

The FDA product code for INSUFFLATOR TUBING is HIG.

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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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