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FDA 510(k)

LASER MIRROR

K-Number: K840982 · 1984-03-06

ApplicantAmerican V. Mueller
Decision Date1984-03-06
Product Code
DecisionUnknown

Device Summary

LASER MIRROR is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1984-03-06 under 510(k) number K840982. FDA Decision: Unknown.

Frequently Asked Questions

What is the LASER MIRROR?

LASER MIRROR is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is American V. Mueller. The 510(k) number is K840982.

When did LASER MIRROR receive FDA 510(k) clearance?

LASER MIRROR received FDA 510(k) clearance on 1984-03-06, under 510(k) number K840982.

Who is the listed applicant for LASER MIRROR?

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

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Other records listing American V. Mueller 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.

K873771HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTROK873332MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEMK871685HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYSK864676HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEMK862772V. MUELLER (R) GOOSENECK CIRCULAR STAPLERK861471V. MUELLER VITAL CLIP-HEMOSTATIC CLIP

View all 31 devices →

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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