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FDA 510(k)

MYCOSEL AGAR

K-Number: K832582 · 1983-09-12

ApplicantAcuderm, Inc.
Decision Date1983-09-12
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MYCOSEL AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Acuderm, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832582. 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 MYCOSEL AGAR?

MYCOSEL AGAR is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Acuderm, Inc.. The 510(k) number is K832582.

When did MYCOSEL AGAR receive FDA 510(k) clearance?

MYCOSEL AGAR received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832582.

Who is the listed applicant for MYCOSEL AGAR?

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

What is the FDA product code for MYCOSEL AGAR?

The FDA product code for MYCOSEL AGAR is JSJ.

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Other records listing Acuderm, 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.

K933516ACU-E PUNCHK933265ACU-DISPO-CE(TM)K933137ACU-SUTURE KITK930043ACU-EVACK933866ACU-HEMOSTATIC RINGK915000ACU-GUARD

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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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