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FDA 510(k)

HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS)

K-Number: K862569 · 1986-08-14

ApplicantJedmed Instrument Co.
Decision Date1986-08-14
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS) is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1986-08-14 under 510(k) number K862569. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS)?

HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS) is a medical device that received FDA 510(k) clearance on 1986-08-14. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K862569.

When did HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS) receive FDA 510(k) clearance?

HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS) received FDA 510(k) clearance on 1986-08-14, under 510(k) number K862569.

Who is the listed applicant for HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS)?

The FDA 510(k) record lists Jedmed Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS)?

The FDA product code for HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS) is BTA.

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Related Devices (Code: BTA)

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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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