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FDA 510(k)

ANIS LENS IMPLANT FORCEPS #2

K-Number: K811658 · 1981-06-26

ApplicantAmerican V. Mueller
Decision Date1981-06-26
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ANIS LENS IMPLANT FORCEPS #2 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 1981-06-26 under 510(k) number K811658. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANIS LENS IMPLANT FORCEPS #2?

ANIS LENS IMPLANT FORCEPS #2 is a medical device that received FDA 510(k) clearance on 1981-06-26. The listed applicant is American V. Mueller. The 510(k) number is K811658.

When did ANIS LENS IMPLANT FORCEPS #2 receive FDA 510(k) clearance?

ANIS LENS IMPLANT FORCEPS #2 received FDA 510(k) clearance on 1981-06-26, under 510(k) number K811658.

Who is the listed applicant for ANIS LENS IMPLANT FORCEPS #2?

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 ANIS LENS IMPLANT FORCEPS #2?

The FDA product code for ANIS LENS IMPLANT FORCEPS #2 is HNR.

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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: HNR)

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.

K022835STEPHENS DISPOSABLE FORCEPSStephens InstrumentsK895434ALCON FOLDING FORCEPSAlcon LaboratoriesK891487SOFT LENS FOLDING BLOCKWestern Medical Products, Inc.K893199PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTRAllergan Medical OpticsK885230MCDONALD FOLDING FORCEPSAlcon LaboratoriesK881049BRADBURY INTRAOCULAR RETINAL KIT CAT #200Microline Pentax, 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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