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)

SCRIBE

K-Number: K924030 · 1993-03-04

ApplicantZygo Industries, Inc.
Decision Date1993-03-04
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCRIBE is the device name listed in this FDA 510(k) record. The listed applicant is Zygo Industries, Inc.. It received FDA 510(k) clearance on 1993-03-04 under 510(k) number K924030. 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 SCRIBE?

SCRIBE is a medical device that received FDA 510(k) clearance on 1993-03-04. The listed applicant is Zygo Industries, Inc.. The 510(k) number is K924030.

When did SCRIBE receive FDA 510(k) clearance?

SCRIBE received FDA 510(k) clearance on 1993-03-04, under 510(k) number K924030.

Who is the listed applicant for SCRIBE?

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

What is the FDA product code for SCRIBE?

The FDA product code for SCRIBE 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 Zygo Industries, 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.

K926029INFRA-LINKK924014SECRETARYK924013MACAWK924015PARROTK862766EPISON, ALERTING SYSTEM FOR EPILEPTICS

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.

↑