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FDA 510(k)

DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR

K-Number: K873447 · 1987-10-30

Decision Date1987-10-30
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR 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 1987-10-30 under 510(k) number K873447. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR?

DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR is a medical device that received FDA 510(k) clearance on 1987-10-30. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K873447.

When did DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR receive FDA 510(k) clearance?

DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR received FDA 510(k) clearance on 1987-10-30, under 510(k) number K873447.

Who is the listed applicant for DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR?

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 DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR?

The FDA product code for DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR is BYH.

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: BYH)

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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