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FDA 510(k)

SAS SPICER-EDWARDS L COMPLEX

K-Number: K955228 · 1996-02-13

ApplicantSa Scientific, Inc.
Decision Date1996-02-13
Product CodeGNC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SAS SPICER-EDWARDS L COMPLEX 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 1996-02-13 under 510(k) number K955228. The device is classified under product code GNC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAS SPICER-EDWARDS L COMPLEX?

SAS SPICER-EDWARDS L COMPLEX is a medical device that received FDA 510(k) clearance on 1996-02-13. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K955228.

When did SAS SPICER-EDWARDS L COMPLEX receive FDA 510(k) clearance?

SAS SPICER-EDWARDS L COMPLEX received FDA 510(k) clearance on 1996-02-13, under 510(k) number K955228.

Who is the listed applicant for SAS SPICER-EDWARDS L COMPLEX?

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 SPICER-EDWARDS L COMPLEX?

The FDA product code for SAS SPICER-EDWARDS L COMPLEX is GNC.

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Other records listing Sa Scientific, Inc. 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.

K100227SAS FLUALERT A&B, SAS INFLUENZA A TESTK080380SAS INFLUENZA A & B TESTK041439SAS INFLUENZA B TESTK041441SAS INFLUENZA A TESTK030628SAS RSV CONTROL KITK022845SAS RSV TEST

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Related Devices (Code: GNC)

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.

K972388VISTA ANTIGEN SALMONELLA O GROUP CLee Laboratories, Inc.K972395VISTA ANTIGEN SALMONELLA O GROUP DLee Laboratories, Inc.K972389VISTA ANTIGEN SALMONELLA H DLee Laboratories, Inc.K972387VISTA ANTIGEN SALMONELLA O GROUP ALee Laboratories, Inc.K972386VISTA ANTIGEN SALMONELLA O GROUP BLee Laboratories, Inc.K972391VISTA ANTIGEN SALMONELLA H BLee Laboratories, Inc.

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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