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FDA 510(k)

APOLLO CAMERA

K-Number: K931136 · 1994-01-11

ApplicantLife Sensing Instrument Company, Inc.
Decision Date1994-01-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

APOLLO CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Life Sensing Instrument Company, Inc.. It received FDA 510(k) clearance on 1994-01-11 under 510(k) number K931136. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APOLLO CAMERA?

APOLLO CAMERA is a medical device that received FDA 510(k) clearance on 1994-01-11. The listed applicant is Life Sensing Instrument Company, Inc.. The 510(k) number is K931136.

When did APOLLO CAMERA receive FDA 510(k) clearance?

APOLLO CAMERA received FDA 510(k) clearance on 1994-01-11, under 510(k) number K931136.

Who is the listed applicant for APOLLO CAMERA?

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

What is the FDA product code for APOLLO CAMERA?

The FDA product code for APOLLO CAMERA is HET.

Related Clinical Trials

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Other records listing Life Sensing Instrument Company, 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.

K960884TELE TRENS TM 10K896967HTS 820 CARDIAC MONITORK884524HTS 220 CARDIAC MONITORK861067PARAGON 420, CARDIAC MONITOR

Related Devices (Code: HET)

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Official Source

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