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FDA 510(k)

DGH A-SAN PROBE HOLDER

K-Number: K900162 · 1990-02-16

ApplicantJedmed Instrument Co.
Decision Date1990-02-16
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DGH A-SAN PROBE HOLDER 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 1990-02-16 under 510(k) number K900162. The device is classified under product code HDR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DGH A-SAN PROBE HOLDER?

DGH A-SAN PROBE HOLDER is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K900162.

When did DGH A-SAN PROBE HOLDER receive FDA 510(k) clearance?

DGH A-SAN PROBE HOLDER received FDA 510(k) clearance on 1990-02-16, under 510(k) number K900162.

Who is the listed applicant for DGH A-SAN PROBE HOLDER?

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 DGH A-SAN PROBE HOLDER?

The FDA product code for DGH A-SAN PROBE HOLDER is HDR.

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Other records listing Jedmed Instrument Co. 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.

K021750LID CHAIN EYELID WEIGHTSK954184JED-LIGHT FIBEROPTIC LIGHT SOURCEK944032VIDEO SCOPE SYSTEM (LARYNGOSCOPE)K953457JEDMED SPECTRUM ENT CABINETK950925JEDMED LARYNGEAL SCOPEK950785HORTMANN AIRMATIC AIR CALORIC STIMULATOR

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Related Devices (Code: HDR)

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.

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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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