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FDA 510(k)

IRON & TICB

K-Number: K810086 · 1981-01-28

ApplicantBio-Analytics Laboratories, Inc.
Decision Date1981-01-28
Product CodeJQF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IRON & TICB is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Analytics Laboratories, Inc.. It received FDA 510(k) clearance on 1981-01-28 under 510(k) number K810086. The device is classified under product code JQF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IRON & TICB?

IRON & TICB is a medical device that received FDA 510(k) clearance on 1981-01-28. The listed applicant is Bio-Analytics Laboratories, Inc.. The 510(k) number is K810086.

When did IRON & TICB receive FDA 510(k) clearance?

IRON & TICB received FDA 510(k) clearance on 1981-01-28, under 510(k) number K810086.

Who is the listed applicant for IRON & TICB?

The FDA 510(k) record lists Bio-Analytics Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IRON & TICB?

The FDA product code for IRON & TICB is JQF.

Other records listing Bio-Analytics Laboratories, Inc. 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.

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Related Devices (Code: JQF)

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.

K051111SENTINEL UIBC LIQUIDSentinel Ch. SrlK984122WAKO L-TYPE UIBC, WAKO UIBC CALIBRATORWako Chemicals USA, Inc.K875176WAKO(TM) UIBCWako Chemicals USA, Inc.K863066TRANSFERMETERJ. D. Assoc.K830032TOTAL IRON BINDING CAPACITY TESTSclavo, Inc.K811942J & S IRON SATURATING REAGENTThyroid Diagnostics, 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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