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FDA 510(k)

MODEL 200 SQUID

K-Number: K822853 · 1982-10-18

ApplicantSynemed, Inc.
Decision Date1982-10-18
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODEL 200 SQUID is the device name listed in this FDA 510(k) record. The listed applicant is Synemed, Inc.. It received FDA 510(k) clearance on 1982-10-18 under 510(k) number K822853. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 200 SQUID?

MODEL 200 SQUID is a medical device that received FDA 510(k) clearance on 1982-10-18. The listed applicant is Synemed, Inc.. The 510(k) number is K822853.

When did MODEL 200 SQUID receive FDA 510(k) clearance?

MODEL 200 SQUID received FDA 510(k) clearance on 1982-10-18, under 510(k) number K822853.

Who is the listed applicant for MODEL 200 SQUID?

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

What is the FDA product code for MODEL 200 SQUID?

The FDA product code for MODEL 200 SQUID is HPT.

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Other records listing Synemed, 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.

K954037FIELD TRENDK852936THE FIELDMASTER MODEL 275K833274DERMATOLOGY HANDPIECE-OPHTH LASERK831085SYNEVAC VACUUM SOURCE UNITK828585OPTHALAS PHOTOCOAGULATORK813282SYNEVAC VACUUM CURETTAGE SYSTEMS

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Related Devices (Code: HPT)

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.

K092187MAIA, MODEL 1Centervue S.P.A.K093213GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIESCarl Zeiss Meditec, Inc.K091579FORESEE HOMENotal Vision , Ltd.K063310TRUEFIELD ANALYZERSeeing Machines LimitedK050350THE NOTAL VISION PREVIEW PREFERENTIAL HYPERACUITY PERIMETER (PREVIEW PHP)Notal Vision, Inc.K023623NOVAVISION, MODEL 2.0Novavision, 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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