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FDA 510(k)

JARIT SURGICAL INSTRUMENTS

K-Number: K932072 · 1994-01-11

ApplicantMedical Device Inspection Co., Inc.
Decision Date1994-01-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JARIT SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1994-01-11 under 510(k) number K932072. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JARIT SURGICAL INSTRUMENTS?

JARIT SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-01-11. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K932072.

When did JARIT SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

JARIT SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1994-01-11, under 510(k) number K932072.

Who is the listed applicant for JARIT SURGICAL INSTRUMENTS?

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

What is the FDA product code for JARIT SURGICAL INSTRUMENTS?

The FDA product code for JARIT SURGICAL INSTRUMENTS is HET.

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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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