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FDA 510(k)

MODEL XA-15 LASER SYSTEM FOR SURGERY

K-Number: K837216 · 1983-04-04

ApplicantXanar, Inc.
Decision Date1983-04-04
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL XA-15 LASER SYSTEM FOR SURGERY is the device name listed in this FDA 510(k) record. The listed applicant is Xanar, Inc.. It received FDA 510(k) clearance on 1983-04-04 under 510(k) number K837216. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL XA-15 LASER SYSTEM FOR SURGERY?

MODEL XA-15 LASER SYSTEM FOR SURGERY is a medical device that received FDA 510(k) clearance on 1983-04-04. The listed applicant is Xanar, Inc.. The 510(k) number is K837216.

When did MODEL XA-15 LASER SYSTEM FOR SURGERY receive FDA 510(k) clearance?

MODEL XA-15 LASER SYSTEM FOR SURGERY received FDA 510(k) clearance on 1983-04-04, under 510(k) number K837216.

Who is the listed applicant for MODEL XA-15 LASER SYSTEM FOR SURGERY?

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

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Other records listing Xanar, 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.

K861688XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15K852436AMBULASEK860496MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARYK853620MODEL XA-50 - CO2 SURGICAL LASERK850804CO 2 SURGICAL LASER SYSTEM NA-30K850805CO 2 SURGICAL LASER SYSTEM MODEL NA-40

View all 12 devices →

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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