FDA 510(k)

SAS HCG SERUM CONTROLS

K-Number: K990720 · 1999-03-19

Decision Date1999-03-19

Product CodeJJX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

SAS HCG SERUM CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Sa Scientific, Inc.. It received FDA 510(k) clearance on 1999-03-19 under 510(k) number K990720. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAS HCG SERUM CONTROLS?

SAS HCG SERUM CONTROLS is a medical device that received FDA 510(k) clearance on 1999-03-19. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K990720.

When did SAS HCG SERUM CONTROLS receive FDA 510(k) clearance?

SAS HCG SERUM CONTROLS received FDA 510(k) clearance on 1999-03-19, under 510(k) number K990720.

Who is the listed applicant for SAS HCG SERUM CONTROLS?

The FDA 510(k) record lists Sa Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAS HCG SERUM CONTROLS?

The FDA product code for SAS HCG SERUM CONTROLS is JJX.

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Other records listing Sa Scientific, Inc. as applicant

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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.