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FDA 510(k)

CAMPYLOBACTER SELECTIVE MEDIUM

K-Number: K820562 · 1982-03-19

ApplicantAmerican Laboratory Supply, Inc.
Decision Date1982-03-19
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CAMPYLOBACTER SELECTIVE MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Supply, Inc.. It received FDA 510(k) clearance on 1982-03-19 under 510(k) number K820562. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPYLOBACTER SELECTIVE MEDIUM?

CAMPYLOBACTER SELECTIVE MEDIUM is a medical device that received FDA 510(k) clearance on 1982-03-19. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K820562.

When did CAMPYLOBACTER SELECTIVE MEDIUM receive FDA 510(k) clearance?

CAMPYLOBACTER SELECTIVE MEDIUM received FDA 510(k) clearance on 1982-03-19, under 510(k) number K820562.

Who is the listed applicant for CAMPYLOBACTER SELECTIVE MEDIUM?

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

What is the FDA product code for CAMPYLOBACTER SELECTIVE MEDIUM?

The FDA product code for CAMPYLOBACTER SELECTIVE MEDIUM is JSJ.

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Other records listing American Laboratory Supply, Inc. as applicant

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Related Devices (Code: JSJ)

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.

K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421Lakewood Biochemical Co., Inc.K881544LITTMAN AGARAcumedia Manufacturers, Inc.K881561TERGITOL 7 BROTHAcumedia Manufacturers, Inc.K881526CHAPMAN STONE MEDIUMAcumedia Manufacturers, Inc.K881571YM BROTHAcumedia Manufacturers, Inc.K881578STREPTOSELAcumedia Manufacturers, 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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