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FDA 510(k)

ALARM INTERCOM DOOR LOCK

K-Number: K770031 · 1977-01-12

ApplicantPossum, Inc.
Decision Date1977-01-12
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ALARM INTERCOM DOOR LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Possum, Inc.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K770031. 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 ALARM INTERCOM DOOR LOCK?

ALARM INTERCOM DOOR LOCK is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Possum, Inc.. The 510(k) number is K770031.

When did ALARM INTERCOM DOOR LOCK receive FDA 510(k) clearance?

ALARM INTERCOM DOOR LOCK received FDA 510(k) clearance on 1977-01-12, under 510(k) number K770031.

Who is the listed applicant for ALARM INTERCOM DOOR LOCK?

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

What is the FDA product code for ALARM INTERCOM DOOR LOCK?

The FDA product code for ALARM INTERCOM DOOR LOCK 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 Possum, 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.

K770028ENVIRONMENTAL CONTROL SYSTEMSK770032PAGE TURNERK770030ALARM, COMMUN.-SEC. INDEP.-EMER.K770029TYPEWRITER CONTROL SYSTEMS

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.

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