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FDA 510(k)

BABY LIGHT METER

K-Number: K837494 · 1983-06-14

ApplicantRocky Mountain Medical Corp.
Decision Date1983-06-14
Product Code
DecisionSubstantially Equivalent

Device Summary

BABY LIGHT METER is the device name listed in this FDA 510(k) record. The listed applicant is Rocky Mountain Medical Corp.. It received FDA 510(k) clearance on 1983-06-14 under 510(k) number K837494. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BABY LIGHT METER?

BABY LIGHT METER is a medical device that received FDA 510(k) clearance on 1983-06-14. The listed applicant is Rocky Mountain Medical Corp.. The 510(k) number is K837494.

When did BABY LIGHT METER receive FDA 510(k) clearance?

BABY LIGHT METER received FDA 510(k) clearance on 1983-06-14, under 510(k) number K837494.

Who is the listed applicant for BABY LIGHT METER?

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

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 Rocky Mountain 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.

K890202TELE-TEMP THERMOMETERK860120NURSERY AMBIENT LIGHT METERK852167ISOVOL-EXCHANGE TRAYK853970ALPHA CHUCKK853790BABE SHADE-INFANT AMBIENT LIGHT INTENSITY REDUCERK851876PREFER INCONTINENCE AID

View all 9 devices →

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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