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FDA 510(k)

H.R. JAKOBI SURG. INSTRUMENTS 40/41

K-Number: K834176 · 1984-01-27

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

Device Summary

H.R. JAKOBI SURG. INSTRUMENTS 40/41 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 K834176. The device is classified under product code GEG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H.R. JAKOBI SURG. INSTRUMENTS 40/41?

H.R. JAKOBI SURG. INSTRUMENTS 40/41 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 K834176.

When did H.R. JAKOBI SURG. INSTRUMENTS 40/41 receive FDA 510(k) clearance?

H.R. JAKOBI SURG. INSTRUMENTS 40/41 received FDA 510(k) clearance on 1984-01-27, under 510(k) number K834176.

Who is the listed applicant for H.R. JAKOBI SURG. INSTRUMENTS 40/41?

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 H.R. JAKOBI SURG. INSTRUMENTS 40/41?

The FDA product code for H.R. JAKOBI SURG. INSTRUMENTS 40/41 is GEG.

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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 DEVICESK841386KOLLMANN URETHRAL DILATORK841387WESTON RECTAL SNAREK840304CATEGORY 17-MICROBIOLOGY DEVICESK840318CAT. 14-CLINICAL TOXIOLOGY DEVICESK840305CATEGORY 1 CIRCULATORY SYSTEM DEVICE

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Related Devices (Code: GEG)

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.

K891899ELEVATORS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.K891894ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSEZinnanti Surgical Instruments, Inc.K890365SEPTUM ELEVATORKinetic Medical ProductsK890230LIGATURE NEEDLESKinetic Medical ProductsK890253SURGICAL ELEVATORKinetic Medical ProductsK8724911.1 TWIST DRILLS AND 1.2 CORTICAL DRILLSMicro-Aire Surgical Instruments, 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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