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FDA 510(k)

JAKOBI SURG. INSTRUMENTS #11

K-Number: K834186 · 1984-01-27

ApplicantImm Enterprises , Ltd.
Decision Date1984-01-27
Product Code
DecisionSubstantially Equivalent

Device Summary

JAKOBI SURG. INSTRUMENTS #11 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 K834186. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAKOBI SURG. INSTRUMENTS #11?

JAKOBI SURG. INSTRUMENTS #11 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 K834186.

When did JAKOBI SURG. INSTRUMENTS #11 receive FDA 510(k) clearance?

JAKOBI SURG. INSTRUMENTS #11 received FDA 510(k) clearance on 1984-01-27, under 510(k) number K834186.

Who is the listed applicant for JAKOBI SURG. INSTRUMENTS #11?

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

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Other records listing Imm Enterprises , Ltd. 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.

K840311CAT. 7-EAR, NOSE & THROAT DEVICESK841387WESTON RECTAL SNAREK841386KOLLMANN URETHRAL DILATORK840304CATEGORY 17-MICROBIOLOGY DEVICESK840318CAT. 14-CLINICAL TOXIOLOGY DEVICESK840305CATEGORY 1 CIRCULATORY SYSTEM DEVICE

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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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