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FDA 510(k)

TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF

K-Number: K925744 · 1993-07-30

ApplicantPymah Corp.
Decision Date1993-07-30
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Pymah Corp.. It received FDA 510(k) clearance on 1993-07-30 under 510(k) number K925744. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF?

TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Pymah Corp.. The 510(k) number is K925744.

When did TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF receive FDA 510(k) clearance?

TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF received FDA 510(k) clearance on 1993-07-30, under 510(k) number K925744.

Who is the listed applicant for TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF?

The FDA 510(k) record lists Pymah Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF?

The FDA product code for TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF is DXQ.

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 Pymah 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 17 devices →

Related Devices (Code: DXQ)

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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