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FDA 510(k)

GATOR DRAPES

K-Number: K811717 · 1981-07-20

ApplicantThe Anspach Effort, Inc.
Decision Date1981-07-20
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GATOR DRAPES is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1981-07-20 under 510(k) number K811717. The device is classified under product code KQM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GATOR DRAPES?

GATOR DRAPES is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K811717.

When did GATOR DRAPES receive FDA 510(k) clearance?

GATOR DRAPES received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811717.

Who is the listed applicant for GATOR DRAPES?

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

What is the FDA product code for GATOR DRAPES?

The FDA product code for GATOR DRAPES is KQM.

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Other records listing The Anspach Effort, 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.

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Related Devices (Code: KQM)

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.

K900160ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTERJedmed Instrument Co.K890826SONY VIDEO GRAPHIC PRINTER UP-850Sony Corp. of AmericaK885042SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MDSony Medical Electronics Co.K882958SONY VIDEO PRINTERS, UP SERIESSony Medical Electronics Co.K882924MEDICAM MC-7 AND RP-7 SURGICAL CAMERASM.P. Video, Inc.K873419VIDEO PRINTER SYSTEMTechnology For Imaging, 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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