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)

CONTROL 1 ENVIRONMENTAL CONTROL

K-Number: K902206 · 1990-05-29

ApplicantPrentke Romich Co.
Decision Date1990-05-29
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONTROL 1 ENVIRONMENTAL CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Prentke Romich Co.. It received FDA 510(k) clearance on 1990-05-29 under 510(k) number K902206. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTROL 1 ENVIRONMENTAL CONTROL?

CONTROL 1 ENVIRONMENTAL CONTROL is a medical device that received FDA 510(k) clearance on 1990-05-29. The listed applicant is Prentke Romich Co.. The 510(k) number is K902206.

When did CONTROL 1 ENVIRONMENTAL CONTROL receive FDA 510(k) clearance?

CONTROL 1 ENVIRONMENTAL CONTROL received FDA 510(k) clearance on 1990-05-29, under 510(k) number K902206.

Who is the listed applicant for CONTROL 1 ENVIRONMENTAL CONTROL?

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

What is the FDA product code for CONTROL 1 ENVIRONMENTAL CONTROL?

The FDA product code for CONTROL 1 ENVIRONMENTAL CONTROL is ILQ.

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 Prentke Romich 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.

K961306DELTATALKER WITH INFRAREDK944585SCANNING DIRECTORK935317ALPHA TALKERK933207WALKERTALKERK925387LIBERATORK925527LIGHT TALKER

View all 9 devices →

Related Devices (Code: ILQ)

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.

K162817Noddle(TM)Iowa Adaptive Technologies, Inc. Dba Voxello, Inc.K943035P.A.T. SYSTEMMathews Assoc., Inc.K930044COMFORT KEYBOARD SYSTEMHealth Care Keyboard Co., Inc.K931855LIGHTWRITERZygo Corp.K935244R & D BATTERIES, INC. PART NUMBER 5113R & D Batteries, Inc.K935981MLT-2Med Labs, 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.

↑