FDA 510(k)

INTERLAB IMMUNOFIXATION TEST(S)

K-Number: K033187 · 2003-11-19

Decision Date2003-11-19

Product CodeCFF

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

INTERLAB IMMUNOFIXATION TEST(S) is the device name listed in this FDA 510(k) record. The listed applicant is Interlab S.R.L.. It received FDA 510(k) clearance on 2003-11-19 under 510(k) number K033187. The device is classified under product code CFF. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERLAB IMMUNOFIXATION TEST(S)?

INTERLAB IMMUNOFIXATION TEST(S) is a medical device that received FDA 510(k) clearance on 2003-11-19. The listed applicant is Interlab S.R.L.. The 510(k) number is K033187.

When did INTERLAB IMMUNOFIXATION TEST(S) receive FDA 510(k) clearance?

INTERLAB IMMUNOFIXATION TEST(S) received FDA 510(k) clearance on 2003-11-19, under 510(k) number K033187.

Who is the listed applicant for INTERLAB IMMUNOFIXATION TEST(S)?

The FDA 510(k) record lists Interlab S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERLAB IMMUNOFIXATION TEST(S)?

The FDA product code for INTERLAB IMMUNOFIXATION TEST(S) is CFF.

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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.