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FDA 510(k)

FASTRECON 88 PERIFERAL

K-Number: K902848 · 1990-08-01

ApplicantScientific Technology , Ltd.
Decision Date1990-08-01
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FASTRECON 88 PERIFERAL is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Technology , Ltd.. It received FDA 510(k) clearance on 1990-08-01 under 510(k) number K902848. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FASTRECON 88 PERIFERAL?

FASTRECON 88 PERIFERAL is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Scientific Technology , Ltd.. The 510(k) number is K902848.

When did FASTRECON 88 PERIFERAL receive FDA 510(k) clearance?

FASTRECON 88 PERIFERAL received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902848.

Who is the listed applicant for FASTRECON 88 PERIFERAL?

The FDA 510(k) record lists Scientific Technology , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FASTRECON 88 PERIFERAL?

The FDA product code for FASTRECON 88 PERIFERAL is JAK.

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Other records listing Scientific Technology , 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.

K926064FLUOROSCOPIC BRIGHTNESS STABALIZER/FBS MODEL 9205A

Related Devices (Code: JAK)

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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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