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FDA 510(k)

ANTI-ASPERGILLUS CONT. SER. (MYCELIAL)

K-Number: K760835 · 1976-11-01

ApplicantI M, Inc.
Decision Date1976-11-01
Product CodeKFG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTI-ASPERGILLUS CONT. SER. (MYCELIAL) is the device name listed in this FDA 510(k) record. The listed applicant is I M, Inc.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760835. The device is classified under product code KFG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-ASPERGILLUS CONT. SER. (MYCELIAL)?

ANTI-ASPERGILLUS CONT. SER. (MYCELIAL) is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is I M, Inc.. The 510(k) number is K760835.

When did ANTI-ASPERGILLUS CONT. SER. (MYCELIAL) receive FDA 510(k) clearance?

ANTI-ASPERGILLUS CONT. SER. (MYCELIAL) received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760835.

Who is the listed applicant for ANTI-ASPERGILLUS CONT. SER. (MYCELIAL)?

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

What is the FDA product code for ANTI-ASPERGILLUS CONT. SER. (MYCELIAL)?

The FDA product code for ANTI-ASPERGILLUS CONT. SER. (MYCELIAL) is KFG.

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 I M, 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.

K914600NEUROLOGICAL SPONGEK892389BIOPSY KITK881363SYRINGE PREFILLED WITH WATERK880753UMBILICAL CORD CLAMPK872741NUTRIPUMPK871495BANDAGES CATALOG NUMBER: 101 TO 220

View all 41 devices →

Related Devices (Code: KFG)

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.

K904499NICOS (NON-INVASIVE CARDIAC OUTPUT SYSTEM)Ackrad LaboratoriesK792698ASPERGILLUS SP, ANTISERUM, POSITIVEMeridian Diagnostics, Inc.K792686ASPERGILLUS SP, ANTISERUM POSITIVEMeridian Diagnostics, Inc.K791386ANTI-ASPERGILLUS (MYCELIAL) CONTR SERUMImmuno-Mycologics, 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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