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FDA 510(k)

AXSYM PHENCYCLIDINE II

K-Number: K953534 · 1995-10-26

ApplicantAbbott Laboratories
Decision Date1995-10-26
Product CodeLCM
DecisionSubstantially Equivalent

Device Summary

AXSYM PHENCYCLIDINE II is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1995-10-26 under 510(k) number K953534. The device is classified under product code LCM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXSYM PHENCYCLIDINE II?

AXSYM PHENCYCLIDINE II is a medical device that received FDA 510(k) clearance on 1995-10-26. The listed applicant is Abbott Laboratories. The 510(k) number is K953534.

When did AXSYM PHENCYCLIDINE II receive FDA 510(k) clearance?

AXSYM PHENCYCLIDINE II received FDA 510(k) clearance on 1995-10-26, under 510(k) number K953534.

Who is the listed applicant for AXSYM PHENCYCLIDINE II?

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

What is the FDA product code for AXSYM PHENCYCLIDINE II?

The FDA product code for AXSYM PHENCYCLIDINE II is LCM.

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Related Devices (Code: LCM)

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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