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FDA 510(k)

TERUMO SENSIBEAD EIA COLORIMETER

K-Number: K854210 · 1985-12-05

ApplicantTerumo Medical Corp.
Decision Date1985-12-05
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TERUMO SENSIBEAD EIA COLORIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1985-12-05 under 510(k) number K854210. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERUMO SENSIBEAD EIA COLORIMETER?

TERUMO SENSIBEAD EIA COLORIMETER is a medical device that received FDA 510(k) clearance on 1985-12-05. The listed applicant is Terumo Medical Corp.. The 510(k) number is K854210.

When did TERUMO SENSIBEAD EIA COLORIMETER receive FDA 510(k) clearance?

TERUMO SENSIBEAD EIA COLORIMETER received FDA 510(k) clearance on 1985-12-05, under 510(k) number K854210.

Who is the listed applicant for TERUMO SENSIBEAD EIA COLORIMETER?

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

What is the FDA product code for TERUMO SENSIBEAD EIA COLORIMETER?

The FDA product code for TERUMO SENSIBEAD EIA COLORIMETER is JJQ.

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Other records listing Terumo Medical Corp. 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.

K111606PINNACLE PRECISION ACCESS SYSTEMK111556GLIDECROSS SUPPORT CATHETERK110540TERUMO SUPPORT CATHETERK102008GLIDESHEATHK091329PINNACLE DESTINATION PERIPHERAL GUIDING SHEATHK082997TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER

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Related Devices (Code: JJQ)

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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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