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FDA 510(k)

INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING

K-Number: K873498 · 1988-03-09

Decision Date1988-03-09
Product CodeBXR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1988-03-09 under 510(k) number K873498. The device is classified under product code BXR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING?

INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K873498.

When did INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING receive FDA 510(k) clearance?

INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING received FDA 510(k) clearance on 1988-03-09, under 510(k) number K873498.

Who is the listed applicant for INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING?

The FDA 510(k) record lists Dhd Medical Products Div. Diemolding Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING?

The FDA product code for INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING is BXR.

Related Clinical Trials

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.

Other records listing Dhd Medical Products Div. Diemolding Corp. as applicant

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.

View all 43 devices →

Related Devices (Code: BXR)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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