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FDA 510(k)

MEDICRAT, HYPODERMIC SYRINGES & NEEDLES

K-Number: K875148 · 1988-02-11

Decision Date1988-02-11
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDICRAT, HYPODERMIC SYRINGES & NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Knowltech Ind., Inc.. It received FDA 510(k) clearance on 1988-02-11 under 510(k) number K875148. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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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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