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FDA 510(k)

FITKIT I CHECKUP KIT

K-Number: K821799 · 1983-08-16

ApplicantPatton, Boggs & Blow
Decision Date1983-08-16
Product CodeCDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FITKIT I CHECKUP KIT is the device name listed in this FDA 510(k) record. The listed applicant is Patton, Boggs & Blow. It received FDA 510(k) clearance on 1983-08-16 under 510(k) number K821799. The device is classified under product code CDM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FITKIT I CHECKUP KIT?

FITKIT I CHECKUP KIT is a medical device that received FDA 510(k) clearance on 1983-08-16. The listed applicant is Patton, Boggs & Blow. The 510(k) number is K821799.

When did FITKIT I CHECKUP KIT receive FDA 510(k) clearance?

FITKIT I CHECKUP KIT received FDA 510(k) clearance on 1983-08-16, under 510(k) number K821799.

Who is the listed applicant for FITKIT I CHECKUP KIT?

The FDA 510(k) record lists Patton, Boggs & Blow as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FITKIT I CHECKUP KIT?

The FDA product code for FITKIT I CHECKUP KIT is CDM.

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Other records listing Patton, Boggs & Blow 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.

K943347KLS MINI OSTEOSYNTHESIS SYSTEMK943346MANUAL SURGICAL INST. AND ACC. TO KLS MINI OSTEOSYNTHESIS SYSTEMK943348KLS CHIN PLATE SYSTEMK943345MANUAL SURGICAL INST. AND ACC. TO KLS CHIN PLATE SYSTEMK823825NOSITE UV INTERIM SPECTACLES

Related Devices (Code: CDM)

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.

K052719URITEST 10 URINALYSIS REAGENT STRIPSArj Medical, Inc.K061559ACON URINALYSIS REAGENT STRIPSAcon Laboratories Co.K880584URI-CHEM(R) GK,2,3,4C,5CN,6C,7C AND 8CMach Diag. C/O Wichita State UniversityK873366WAKO(TM) PRETEST 5AWako Chemicals USA, Inc.K852611TEST UROBILINOGEN IN URINE & LEUKOCYTES IN URINEMiles Laboratories, Inc.K830340FITKIT I CHECKUP KITBoditestor

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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