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FDA 510(k)

CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM.

K-Number: K781602 · 1978-10-10

ApplicantAnaerobe Systems
Decision Date1978-10-10
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM. is the device name listed in this FDA 510(k) record. The listed applicant is Anaerobe Systems. It received FDA 510(k) clearance on 1978-10-10 under 510(k) number K781602. 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 CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM.?

CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM. is a medical device that received FDA 510(k) clearance on 1978-10-10. The listed applicant is Anaerobe Systems. The 510(k) number is K781602.

When did CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM. receive FDA 510(k) clearance?

CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM. received FDA 510(k) clearance on 1978-10-10, under 510(k) number K781602.

Who is the listed applicant for CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM.?

The FDA 510(k) record lists Anaerobe Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM.?

The FDA product code for CDC ANAEROBE BLOOD W/KANAMYAN/VANCOM. is JSJ.

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Other records listing Anaerobe Systems 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.

K844381COLISTIN 10 MCG. DIFFERENTIAL DISKK844382VANCOMYCIN 5MCG DIFFERENTIAL DISKK844380BILE DIFFERENTIAL DISKK844383KANAMYCIN 1000 MCG DIFFERENTIAL DISKK841303CAMPYLOBACTER THIOGLYCOLLATE MEDK841142LEVINE EOSIN METHYLENE BLUE AGAR

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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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