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FDA 510(k)

PYMAH PRE-GAGED BALANCED TEMPA-KUFF

K-Number: K903379 · 1990-10-19

ApplicantPymah Corp.
Decision Date1990-10-19
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PYMAH PRE-GAGED BALANCED TEMPA-KUFF is the device name listed in this FDA 510(k) record. The listed applicant is Pymah Corp.. It received FDA 510(k) clearance on 1990-10-19 under 510(k) number K903379. 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 PYMAH PRE-GAGED BALANCED TEMPA-KUFF?

PYMAH PRE-GAGED BALANCED TEMPA-KUFF is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is Pymah Corp.. The 510(k) number is K903379.

When did PYMAH PRE-GAGED BALANCED TEMPA-KUFF receive FDA 510(k) clearance?

PYMAH PRE-GAGED BALANCED TEMPA-KUFF received FDA 510(k) clearance on 1990-10-19, under 510(k) number K903379.

Who is the listed applicant for PYMAH PRE-GAGED BALANCED TEMPA-KUFF?

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 PYMAH PRE-GAGED BALANCED TEMPA-KUFF?

The FDA product code for PYMAH PRE-GAGED BALANCED TEMPA-KUFF 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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