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FDA 510(k)

JEDMED MICRO CCD CAMERA SYSTEM

K-Number: K882166 · 1988-06-15

Decision Date1988-06-15
Product CodeFWD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JEDMED MICRO CCD CAMERA SYSTEM 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 1988-06-15 under 510(k) number K882166. The device is classified under product code FWD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JEDMED MICRO CCD CAMERA SYSTEM?

JEDMED MICRO CCD CAMERA SYSTEM is a medical device that received FDA 510(k) clearance on 1988-06-15. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K882166.

When did JEDMED MICRO CCD CAMERA SYSTEM receive FDA 510(k) clearance?

JEDMED MICRO CCD CAMERA SYSTEM received FDA 510(k) clearance on 1988-06-15, under 510(k) number K882166.

Who is the listed applicant for JEDMED MICRO CCD CAMERA SYSTEM?

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 JEDMED MICRO CCD CAMERA SYSTEM?

The FDA product code for JEDMED MICRO CCD CAMERA SYSTEM is FWD.

Related Clinical Trials

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.

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.

View all 91 devices →

Related Devices (Code: FWD)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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