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FDA 510(k)

CHAMBER V-9 PLUS AGAR

K-Number: K851238 · 1985-05-29

ApplicantBug City Company, Inc.
Decision Date1985-05-29
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHAMBER V-9 PLUS AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Bug City Company, Inc.. It received FDA 510(k) clearance on 1985-05-29 under 510(k) number K851238. 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 CHAMBER V-9 PLUS AGAR?

CHAMBER V-9 PLUS AGAR is a medical device that received FDA 510(k) clearance on 1985-05-29. The listed applicant is Bug City Company, Inc.. The 510(k) number is K851238.

When did CHAMBER V-9 PLUS AGAR receive FDA 510(k) clearance?

CHAMBER V-9 PLUS AGAR received FDA 510(k) clearance on 1985-05-29, under 510(k) number K851238.

Who is the listed applicant for CHAMBER V-9 PLUS AGAR?

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

What is the FDA product code for CHAMBER V-9 PLUS AGAR?

The FDA product code for CHAMBER V-9 PLUS AGAR is JSJ.

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Related Devices (Code: JSJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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