Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONFIRMATION TESTS

K-Number: K873907 · 1987-12-29

ApplicantRichmond Products, Inc.
Decision Date1987-12-29
Product CodeHPC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONFIRMATION TESTS is the device name listed in this FDA 510(k) record. The listed applicant is Richmond Products, Inc.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K873907. The device is classified under product code HPC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONFIRMATION TESTS?

CONFIRMATION TESTS is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Richmond Products, Inc.. The 510(k) number is K873907.

When did CONFIRMATION TESTS receive FDA 510(k) clearance?

CONFIRMATION TESTS received FDA 510(k) clearance on 1987-12-29, under 510(k) number K873907.

Who is the listed applicant for CONFIRMATION TESTS?

The FDA 510(k) record lists Richmond Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONFIRMATION TESTS?

The FDA product code for CONFIRMATION TESTS is HPC.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Richmond Products, 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.

K874252KREDA DISCK874250THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.K874251WORTH 4 DOT TEST DISTANCE C/W MUSCLE LIGHTK873908H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.K873914ANIMATED FIXATION TOYS (DISTANCE AND NEARPOINT)K873916'E' CUBE AND 'E' PAD

View all 15 devices →

Related Devices (Code: HPC)

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.

K945443BOBES LENS SETBobes S.A.K951437OTI MODEL TLS-60Oti Medical, LLCK930195OPHTHALMIC TRIAL LENSESOptimark Accessories and InstrumentsK934859CONTACT LENSESArno Intl., Inc.K930446MARCO TRIAL SETSMarco Ophthalmic, Inc.K924786BURTON TRIAL LENS SETR.H. Burton Co.

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.

↑