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FDA 510(k)

ANIS IRRIGATING SPATULA

K-Number: K810937 · 1981-05-15

ApplicantAmerican V. Mueller
Decision Date1981-05-15
Product CodeHND
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ANIS IRRIGATING SPATULA 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 1981-05-15 under 510(k) number K810937. The device is classified under product code HND. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANIS IRRIGATING SPATULA?

ANIS IRRIGATING SPATULA is a medical device that received FDA 510(k) clearance on 1981-05-15. The listed applicant is American V. Mueller. The 510(k) number is K810937.

When did ANIS IRRIGATING SPATULA receive FDA 510(k) clearance?

ANIS IRRIGATING SPATULA received FDA 510(k) clearance on 1981-05-15, under 510(k) number K810937.

Who is the listed applicant for ANIS IRRIGATING SPATULA?

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 IRRIGATING SPATULA?

The FDA product code for ANIS IRRIGATING SPATULA is HND.

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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: HND)

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.

K863990THORNTON TITANIUM SILVER SPATULAKeeler Instruments, Inc.K801609MADDOX LENS SPATULA CAT. #7245Edward Weck, Inc.K801608MCCULLEY CONTINUOUS SUTURE TIGHTNEREdward Weck, Inc.K791983SPATULA'S #'S 7618,7248,7240,7242,5108Edward Weck, Inc.K761253CYCLODIALYSIS SPAT. 15MM BLADE TITANIUMEdward Weck, 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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