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FDA 510(k)

MODEL ASYM-100

K-Number: K930213 · 1993-09-07

ApplicantNucletron Mfg. Corp.
Decision Date1993-09-07
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL ASYM-100 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Mfg. Corp.. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K930213. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL ASYM-100?

MODEL ASYM-100 is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Nucletron Mfg. Corp.. The 510(k) number is K930213.

When did MODEL ASYM-100 receive FDA 510(k) clearance?

MODEL ASYM-100 received FDA 510(k) clearance on 1993-09-07, under 510(k) number K930213.

Who is the listed applicant for MODEL ASYM-100?

The FDA 510(k) record lists Nucletron Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL ASYM-100?

The FDA product code for MODEL ASYM-100 is KPQ.

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Related Devices (Code: KPQ)

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

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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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