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FDA 510(k)

QUARTZ RETRACTOR/PROBE

K-Number: K823792 · 1983-01-18

ApplicantAmerican V. Mueller
Decision Date1983-01-18
Product CodeKOH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

QUARTZ RETRACTOR/PROBE 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 1983-01-18 under 510(k) number K823792. The device is classified under product code KOH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUARTZ RETRACTOR/PROBE?

QUARTZ RETRACTOR/PROBE is a medical device that received FDA 510(k) clearance on 1983-01-18. The listed applicant is American V. Mueller. The 510(k) number is K823792.

When did QUARTZ RETRACTOR/PROBE receive FDA 510(k) clearance?

QUARTZ RETRACTOR/PROBE received FDA 510(k) clearance on 1983-01-18, under 510(k) number K823792.

Who is the listed applicant for QUARTZ RETRACTOR/PROBE?

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

What is the FDA product code for QUARTZ RETRACTOR/PROBE?

The FDA product code for QUARTZ RETRACTOR/PROBE is KOH.

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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

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Related Devices (Code: KOH)

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.

K000212KSEA CHARDONNES MORCELLATION KNIFEKARL STORZ Endoscopy-America, Inc.K921730C-SECTION PACKMedikmark, Inc.K921732MINOR LAP SETMedikmark, Inc.K892693VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTZinnanti Surgical Instruments, Inc.K891351NEWPORT LATERAL VAGINAL RETRACTORSimpson/Basye, Inc.K891035NEEDLE EXTENSIONSZinnanti Surgical Instruments, Inc.

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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