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FDA 510(k)

ROTARY COMMUNICATION SCANNER MODEL 7010

K-Number: K901030 · 1990-03-13

ApplicantBaylor Biomedical Services
Decision Date1990-03-13
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ROTARY COMMUNICATION SCANNER MODEL 7010 is the device name listed in this FDA 510(k) record. The listed applicant is Baylor Biomedical Services. It received FDA 510(k) clearance on 1990-03-13 under 510(k) number K901030. 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 ROTARY COMMUNICATION SCANNER MODEL 7010?

ROTARY COMMUNICATION SCANNER MODEL 7010 is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is Baylor Biomedical Services. The 510(k) number is K901030.

When did ROTARY COMMUNICATION SCANNER MODEL 7010 receive FDA 510(k) clearance?

ROTARY COMMUNICATION SCANNER MODEL 7010 received FDA 510(k) clearance on 1990-03-13, under 510(k) number K901030.

Who is the listed applicant for ROTARY COMMUNICATION SCANNER MODEL 7010?

The FDA 510(k) record lists Baylor Biomedical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROTARY COMMUNICATION SCANNER MODEL 7010?

The FDA product code for ROTARY COMMUNICATION SCANNER MODEL 7010 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.

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Other records listing Baylor Biomedical Services 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.

K901029YES-NO VOICE BOX 7011K901028ENVIRONMENTAL CONTROL UNIT MODEL 7000K900969REMOTE CONTROL SWITCH

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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