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FDA 510(k)

PRECEPT MICRO-GARD LASER MASK

K-Number: K891409 · 1989-04-07

Decision Date1989-04-07
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRECEPT MICRO-GARD LASER MASK is the device name listed in this FDA 510(k) record. The listed applicant is Mars White Knight. It received FDA 510(k) clearance on 1989-04-07 under 510(k) number K891409. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECEPT MICRO-GARD LASER MASK?

PRECEPT MICRO-GARD LASER MASK is a medical device that received FDA 510(k) clearance on 1989-04-07. The listed applicant is Mars White Knight. The 510(k) number is K891409.

When did PRECEPT MICRO-GARD LASER MASK receive FDA 510(k) clearance?

PRECEPT MICRO-GARD LASER MASK received FDA 510(k) clearance on 1989-04-07, under 510(k) number K891409.

Who is the listed applicant for PRECEPT MICRO-GARD LASER MASK?

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

What is the FDA product code for PRECEPT MICRO-GARD LASER MASK?

The FDA product code for PRECEPT MICRO-GARD LASER MASK is FXX.

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.

Related Devices (Code: FXX)

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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