MEDICRAT, HYPODERMIC SYRINGES & NEEDLES
K-Number: K875148 · 1988-02-11
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Device Summary
Frequently Asked Questions
What is the MEDICRAT, HYPODERMIC SYRINGES & NEEDLES?
MEDICRAT, HYPODERMIC SYRINGES & NEEDLES is a medical device that received FDA 510(k) clearance on 1988-02-11. The listed applicant is Knowltech Ind., Inc.. The 510(k) number is K875148.
When did MEDICRAT, HYPODERMIC SYRINGES & NEEDLES receive FDA 510(k) clearance?
MEDICRAT, HYPODERMIC SYRINGES & NEEDLES received FDA 510(k) clearance on 1988-02-11, under 510(k) number K875148.
Who is the listed applicant for MEDICRAT, HYPODERMIC SYRINGES & NEEDLES?
The FDA 510(k) record lists Knowltech Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDICRAT, HYPODERMIC SYRINGES & NEEDLES?
The FDA product code for MEDICRAT, HYPODERMIC SYRINGES & NEEDLES is FMF.
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.
Related Devices (Code: FMF)
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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