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FDA 510(k)

V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES

K-Number: K851082 · 1985-07-22

ApplicantAmerican V. Mueller
Decision Date1985-07-22
Product CodeENW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES 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 1985-07-22 under 510(k) number K851082. The device is classified under product code ENW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES?

V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES is a medical device that received FDA 510(k) clearance on 1985-07-22. The listed applicant is American V. Mueller. The 510(k) number is K851082.

When did V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES receive FDA 510(k) clearance?

V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES received FDA 510(k) clearance on 1985-07-22, under 510(k) number K851082.

Who is the listed applicant for V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES?

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 BLOM-SINGER ESOPHAGEAL INSUFFLATION TES?

The FDA product code for V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES is ENW.

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Related Devices (Code: ENW)

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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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