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FDA 510(k)

QUALICHECK TM

K-Number: K771444 · 1977-08-16

ApplicantThe London Co.
Decision Date1977-08-16
Product CodeJJS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUALICHECK TM is the device name listed in this FDA 510(k) record. The listed applicant is The London Co.. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771444. The device is classified under product code JJS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUALICHECK TM?

QUALICHECK TM is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is The London Co.. The 510(k) number is K771444.

When did QUALICHECK TM receive FDA 510(k) clearance?

QUALICHECK TM received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771444.

Who is the listed applicant for QUALICHECK TM?

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

What is the FDA product code for QUALICHECK TM?

The FDA product code for QUALICHECK TM is JJS.

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Other records listing The London 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.

K802846TCM202 TCPO2 & TCM204 TCPO2/PO2 REC. SY.K801848ICA1 IONIZED CALCIUM ANALYZERK800224RADIOMETER ACID BASE LABORATORY-ABL-3K780652HEMOGLOBIN CHECK SOLUTIONS, S2100 OSM-2K771263RADIOMHTER OSM-2 HEMOXIMETERK760229ACID BASE SYSTEM, RADIOMETER AUTOMATED

View all 7 devices →

Related Devices (Code: JJS)

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.

K152553CueSee HypoxicEurotrol B.V.K130415HIGH METABOLITE QUALICHECKRadiometer Medical ApsK130236RANGE + QUALICHECK LEVEL 1, RANGE + QUALICHECK LEVEL 2, RANGE + QUALICHECK LEVEL 3Radiometer Medical ApsK033063MISSION CONTROLSDiamond Diagnostics, Inc.K022525LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (RADIOMETER 700 SERIES) LEVELS, 1,2 AND 3, MODEL 507, 508, 509Bio-RadK022529LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (IL SYNTHESIS SERIES) LEVELS 1,2, AND 3, MODELS 667,668,669Bio-Rad

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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