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FDA 510(k)

DHD ACE WITH MASK KIT

K-Number: K961973 · 1996-08-15

Decision Date1996-08-15
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DHD ACE WITH MASK KIT is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Diemolding Healthcare Div.. It received FDA 510(k) clearance on 1996-08-15 under 510(k) number K961973. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DHD ACE WITH MASK KIT?

DHD ACE WITH MASK KIT is a medical device that received FDA 510(k) clearance on 1996-08-15. The listed applicant is Dhd Diemolding Healthcare Div.. The 510(k) number is K961973.

When did DHD ACE WITH MASK KIT receive FDA 510(k) clearance?

DHD ACE WITH MASK KIT received FDA 510(k) clearance on 1996-08-15, under 510(k) number K961973.

Who is the listed applicant for DHD ACE WITH MASK KIT?

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

What is the FDA product code for DHD ACE WITH MASK KIT?

The FDA product code for DHD ACE WITH MASK KIT is CAF.

Other records listing Dhd Diemolding Healthcare Div. 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 11 devices →

Related Devices (Code: CAF)

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

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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