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FDA 510(k)

PRESSURE MODULES MODELS 1855 & 1856

K-Number: K780541 · 1978-05-19

ApplicantLife-Tech Instruments, Inc.
Decision Date1978-05-19
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PRESSURE MODULES MODELS 1855 & 1856 is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Instruments, Inc.. It received FDA 510(k) clearance on 1978-05-19 under 510(k) number K780541. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE MODULES MODELS 1855 & 1856?

PRESSURE MODULES MODELS 1855 & 1856 is a medical device that received FDA 510(k) clearance on 1978-05-19. The listed applicant is Life-Tech Instruments, Inc.. The 510(k) number is K780541.

When did PRESSURE MODULES MODELS 1855 & 1856 receive FDA 510(k) clearance?

PRESSURE MODULES MODELS 1855 & 1856 received FDA 510(k) clearance on 1978-05-19, under 510(k) number K780541.

Who is the listed applicant for PRESSURE MODULES MODELS 1855 & 1856?

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

What is the FDA product code for PRESSURE MODULES MODELS 1855 & 1856?

The FDA product code for PRESSURE MODULES MODELS 1855 & 1856 is IKN.

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Other records listing Life-Tech Instruments, 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.

K812177LIFE-TECH #1857 PRESSURE/POLOT MODULEK812179LIFE-TECH #1753 BIOFEEDBACK TRAINERK812180LIFE-TECH #5102 VISULABK812178LIFE-TECH #'S 1106/1156 UROLABSK800112AMBLYOPIA TRAINERK790663MODEL 1750 STANDING URINAL

View all 19 devices →

Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, 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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