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FDA 510(k)

INTERSPEC APOGEE CLA

K-Number: K924231 · 1993-06-14

ApplicantInterspec, Inc.
Decision Date1993-06-14
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERSPEC APOGEE CLA is the device name listed in this FDA 510(k) record. The listed applicant is Interspec, Inc.. It received FDA 510(k) clearance on 1993-06-14 under 510(k) number K924231. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSPEC APOGEE CLA?

INTERSPEC APOGEE CLA is a medical device that received FDA 510(k) clearance on 1993-06-14. The listed applicant is Interspec, Inc.. The 510(k) number is K924231.

When did INTERSPEC APOGEE CLA receive FDA 510(k) clearance?

INTERSPEC APOGEE CLA received FDA 510(k) clearance on 1993-06-14, under 510(k) number K924231.

Who is the listed applicant for INTERSPEC APOGEE CLA?

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

What is the FDA product code for INTERSPEC APOGEE CLA?

The FDA product code for INTERSPEC APOGEE CLA is IYO.

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Other records listing Interspec, Inc. 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.

K940671INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND FLOWMETERK915696INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDEK920678ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETERK911073PROBE REFILL KITK910049INTERSPEC APOGEE, MODIFICATIONK903839INTERSPEC APOGEE

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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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