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FDA 510(k)

CUFFCHECK

K-Number: K881178 · 1988-04-14

ApplicantDhd Medical Products Div. Diemolding Corp.
Decision Date1988-04-14
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CUFFCHECK 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 1988-04-14 under 510(k) number K881178. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUFFCHECK?

CUFFCHECK is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K881178.

When did CUFFCHECK receive FDA 510(k) clearance?

CUFFCHECK received FDA 510(k) clearance on 1988-04-14, under 510(k) number K881178.

Who is the listed applicant for CUFFCHECK?

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 CUFFCHECK?

The FDA product code for CUFFCHECK is BSK.

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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.

K883988NON-REBREATHING TEE PIECE (NRTP)K881935MICROCIRRUS MEDICAL NEBULIZERK873498INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBINGK874047ASTHMAKITK873447DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATORK860882DISPOSABLE CATHETER

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Related Devices (Code: BSK)

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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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