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FDA 510(k)

V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET

K-Number: K844628 · 1984-12-14

ApplicantAmerican V. Mueller
Decision Date1984-12-14
Product CodeGAG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET 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 1984-12-14 under 510(k) number K844628. The device is classified under product code GAG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET?

V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET is a medical device that received FDA 510(k) clearance on 1984-12-14. The listed applicant is American V. Mueller. The 510(k) number is K844628.

When did V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET receive FDA 510(k) clearance?

V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET received FDA 510(k) clearance on 1984-12-14, under 510(k) number K844628.

Who is the listed applicant for V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET?

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 V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET?

The FDA product code for V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET is GAG.

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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: GAG)

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.

K253527Tri-Staple™ 2.0 Black Circular Reload 21mm Extra Thick (SIGCIR21XT); Tri-Staple™ 2.0 Black Circular Reload 25mm Extra Thick (SIGCIR25XT)Covidien, LLCK251482AEON™ Endoscopic Powered StaplerLexington Medical, Inc.K243596da Vinci SP SureForm 45 Staplers and Reloads (SP1098)Intuitive Surgical, Inc.K240881Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL)Covidien (Part of Medtronic)K241629ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler (ECH45S); Echelon 3000 45mm Long Stapler (ECH45L); Echelon 3000 60mm Compact Stapler (ECH60C); Echelon 3000 60mm Standard Stapler (ECH60S); Echelon 3000 60mm Long Stapler (ECH60L)Ethicon Endo-Surgery, LLCK234039AEON Endoscopic Powered Stapler (Short/AEPH060); AEON Endoscopic Powered Stapler (Medium/AEPH160); AEON Endoscopic Powered Stapler (Long/AEPH260)Lexington Medical, 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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