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FDA 510(k)

TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO

K-Number: K831245 · 1983-10-19

ApplicantRitter Co.
Decision Date1983-10-19
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO is the device name listed in this FDA 510(k) record. The listed applicant is Ritter Co.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K831245. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO?

TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Ritter Co.. The 510(k) number is K831245.

When did TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO receive FDA 510(k) clearance?

TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO received FDA 510(k) clearance on 1983-10-19, under 510(k) number K831245.

Who is the listed applicant for TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO?

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

What is the FDA product code for TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO?

The FDA product code for TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO is DXN.

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Other records listing Ritter Co. 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.

K832171SELF CHECK DIGITAL BLOOD PRESS. MONITORK831976POWER OPTICK823180SA-21 DENTAL UNITK800084RITTER MODEL J DENTAL CHAIRK781101ELECTROSURGICAL UNIT 75K780293ELECTROSURGICAL UNIT

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Related Devices (Code: DXN)

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.

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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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