Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

W-L DIFFERENTIAL MEDIUM

K-Number: K881574 · 1988-04-18

ApplicantAcumedia Manufacturers, Inc.
Decision Date1988-04-18
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

W-L DIFFERENTIAL MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Acumedia Manufacturers, Inc.. It received FDA 510(k) clearance on 1988-04-18 under 510(k) number K881574. 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 W-L DIFFERENTIAL MEDIUM?

W-L DIFFERENTIAL MEDIUM is a medical device that received FDA 510(k) clearance on 1988-04-18. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K881574.

When did W-L DIFFERENTIAL MEDIUM receive FDA 510(k) clearance?

W-L DIFFERENTIAL MEDIUM received FDA 510(k) clearance on 1988-04-18, under 510(k) number K881574.

Who is the listed applicant for W-L DIFFERENTIAL MEDIUM?

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

What is the FDA product code for W-L DIFFERENTIAL MEDIUM?

The FDA product code for W-L DIFFERENTIAL MEDIUM is JSJ.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Acumedia Manufacturers, 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.

K881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGARK881540FLO AGARK881544LITTMAN AGARK881561TERGITOL 7 BROTHK881575SELECTIVE STREPTOCOCCUS AGARK881569STUARTS TRANSPORT MEDIUM

View all 177 devices →

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.

↑