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FDA 510(k)

JAKOBI SURG. INSTRUMENTS #11 20/25/27/37

K-Number: K834196 · 1984-01-27

ApplicantImm Enterprises , Ltd.
Decision Date1984-01-27
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JAKOBI SURG. INSTRUMENTS #11 20/25/27/37 is the device name listed in this FDA 510(k) record. The listed applicant is Imm Enterprises , Ltd.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K834196. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAKOBI SURG. INSTRUMENTS #11 20/25/27/37?

JAKOBI SURG. INSTRUMENTS #11 20/25/27/37 is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Imm Enterprises , Ltd.. The 510(k) number is K834196.

When did JAKOBI SURG. INSTRUMENTS #11 20/25/27/37 receive FDA 510(k) clearance?

JAKOBI SURG. INSTRUMENTS #11 20/25/27/37 received FDA 510(k) clearance on 1984-01-27, under 510(k) number K834196.

Who is the listed applicant for JAKOBI SURG. INSTRUMENTS #11 20/25/27/37?

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

What is the FDA product code for JAKOBI SURG. INSTRUMENTS #11 20/25/27/37?

The FDA product code for JAKOBI SURG. INSTRUMENTS #11 20/25/27/37 is GAD.

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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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