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FDA 510(k)

SALMONELLA & SHIGELLA GROUPING SERA

K-Number: K820996 · 1982-05-03

ApplicantFisher Scientific Co., LLC
Decision Date1982-05-03
Product CodeGRL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SALMONELLA & SHIGELLA GROUPING SERA is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K820996. The device is classified under product code GRL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALMONELLA & SHIGELLA GROUPING SERA?

SALMONELLA & SHIGELLA GROUPING SERA is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K820996.

When did SALMONELLA & SHIGELLA GROUPING SERA receive FDA 510(k) clearance?

SALMONELLA & SHIGELLA GROUPING SERA received FDA 510(k) clearance on 1982-05-03, under 510(k) number K820996.

Who is the listed applicant for SALMONELLA & SHIGELLA GROUPING SERA?

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

What is the FDA product code for SALMONELLA & SHIGELLA GROUPING SERA?

The FDA product code for SALMONELLA & SHIGELLA GROUPING SERA is GRL.

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Other records listing Fisher Scientific Co., LLC 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.

K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

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Related Devices (Code: GRL)

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.

K945839SAS(TM) QC ANTIGENS FOR SALMONELLA ANTISERASa Scientific, 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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