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FDA 510(k)

ALARM, COMMUN.-SEC. INDEP.-EMER.

K-Number: K770030 · 1977-01-12

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

Device Summary

ALARM, COMMUN.-SEC. INDEP.-EMER. 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 K770030. 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, COMMUN.-SEC. INDEP.-EMER.?

ALARM, COMMUN.-SEC. INDEP.-EMER. 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 K770030.

When did ALARM, COMMUN.-SEC. INDEP.-EMER. receive FDA 510(k) clearance?

ALARM, COMMUN.-SEC. INDEP.-EMER. received FDA 510(k) clearance on 1977-01-12, under 510(k) number K770030.

Who is the listed applicant for ALARM, COMMUN.-SEC. INDEP.-EMER.?

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, COMMUN.-SEC. INDEP.-EMER.?

The FDA product code for ALARM, COMMUN.-SEC. INDEP.-EMER. 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 TURNERK770029TYPEWRITER CONTROL SYSTEMSK770031ALARM INTERCOM DOOR LOCK

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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