PYMAH PRE-GAGED BALANCED TEMPA-KUFF
K-Number: K903379 · 1990-10-19
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Device Summary
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.
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
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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